Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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