Variant report

Variant	rs7157918
Chromosome Location	chr14:69641807-69641808
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11158795	0.83[GIH][hapmap]
rs11628353	0.91[AFR][1000 genomes]
rs12432645	0.82[CHB][hapmap];0.91[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12586650	0.91[CHB][hapmap];0.93[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.90[AFR][1000 genomes]
rs12587583	0.91[CHB][hapmap];0.89[GIH][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];0.88[TSI][hapmap];1.00[AFR][1000 genomes]
rs12889047	1.00[AFR][1000 genomes]
rs12894822	0.82[CHB][hapmap];0.89[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.90[AFR][1000 genomes]
rs17758220	1.00[AFR][1000 genomes]
rs3211166	0.81[GIH][hapmap]
rs34227963	1.00[AFR][1000 genomes]
rs34471700	0.91[AFR][1000 genomes]
rs35286356	1.00[AFR][1000 genomes]
rs7151437	0.91[AFR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7157918	WDR22	Cis_1M	lymphoblastoid	RTeQTL

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