Original source

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

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

Chromosome 17:7673766 (forward strand)|View in location tab

Co-located variants
Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 5934

HGVS names

This variant has 73 HGVS names - Show

About this variant

This variant overlaps 43 transcripts and is associated with 3 phenotypes.

Variant displays