Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (T)

Chromosome 12:1913567 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17223603, rs58820222

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2851 sample genotypes.

Variant displays