Variant report

Variant	rs10255159
Chromosome Location	chr7:104236913-104236914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10266389	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10270888	0.90[YRI][hapmap]
rs10272959	0.82[LWK][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs12705235	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1465342	0.81[YRI][hapmap]
rs1468864	0.81[YRI][hapmap]
rs1548938	0.80[YRI][hapmap]
rs1861611	1.00[MEX][hapmap]
rs2193200	0.81[YRI][hapmap]
rs2193213	1.00[EUR][1000 genomes]
rs2216245	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs2385238	0.80[YRI][hapmap]
rs2385245	1.00[MEX][hapmap]
rs2385254	0.81[YRI][hapmap]
rs4727607	1.00[MEX][hapmap];1.00[EUR][1000 genomes]
rs6969085	1.00[MEX][hapmap]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10255159	ALDH2	trans	lymphoblastoid	seeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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