Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.17 (A)
Location

Chromosome 6:43626722 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61227907

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2508 sample genotypes.

Variant displays