Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 17:47573669 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs16970340, rs3179529

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays