Original source

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

G/A|Ancestral: A|Ambiguity code: R|MAF: 0.46 (G)

Chromosome 17:43122889 (forward strand)|View in location tab

Co-located variant

dbSNP rs199839105 (G/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1180358, rs8176084

HGVS names

This variant has 25 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and has 2608 sample genotypes.

Variant displays