Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60290047, rs3730213

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2804 individual genotypes.

Variation displays