Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.45 (G)
Location

Chromosome 7:31095890 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs10386990, rs56702131

HGVS names

This variant has 7 HGVS names - Hide

7:g.31095890C>G
ENST00000409363.5:c.983+3155C>G
ENST00000409489.5:c.1130+140C>G
ENST00000614107.4:c.1046+3155C>G
ENST00000304166.8:c.1046+3155C>G
ENST00000396211.6:c.1046+3155C>G
ENST00000436116.1:c.279+140C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 6 transcripts, has 3693 sample genotypes and is mentioned in 17 citations.

Variant displays