Original source

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

T/A/C|Ancestral: T|Ambiguity code: H

Chromosome 17:7669572 (forward strand)|View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 74 HGVS names - Show

About this variant

This variant overlaps 80 transcripts and is mentioned in 1 citation.

Variant displays