Original source

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

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

Chromosome 17:50185622 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs11556515

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2 sample genotypes.

Variant displays