Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 3:129059424 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59925963

HGVS name

3:g.129059424T>C

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2530 individual genotypes.

Variation displays