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 72 HGVS names - Show

About this variant

This variant overlaps 78 transcripts and is mentioned in 1 citation.

Variant displays