Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 17:47562764 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2010995

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts.

Variant displays