Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.20 (C)

Chromosome 17:2801387 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1269989, rs810043

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2508 sample genotypes.

Variant displays