Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)

Chromosome 1:115287199 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60290047, rs3730213

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2804 sample genotypes.

Variant displays