Variant report

Variant	rs7798500
Chromosome Location	chr7:106662083-106662084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12113322	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17153745	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56132452	0.87[ASN][1000 genomes]
rs56266717	0.87[ASN][1000 genomes]
rs60714435	0.87[ASN][1000 genomes]
rs6954575	0.83[GIH][hapmap];0.86[EUR][1000 genomes]
rs73413319	0.87[ASN][1000 genomes]
rs73413321	0.87[ASN][1000 genomes]
rs73413323	0.87[ASN][1000 genomes]
rs73413330	0.87[ASN][1000 genomes]
rs73413336	0.87[ASN][1000 genomes]
rs73413342	0.87[ASN][1000 genomes]
rs7795821	0.86[EUR][1000 genomes]
rs7807247	0.86[EUR][1000 genomes]
rs849304	0.86[EUR][1000 genomes]

Variant related diseases (count:1)

Disease	PMID	Source
Adverse response to lamotrigine and phenytoin	22379998	GWAS catalog

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106662000-106662400	Enhancers	K562	blood

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links