Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.44 (A)
Location

Chromosome 7:134536942 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1626996, rs10353016

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2578 sample genotypes.

Variant displays