Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 1:229282184 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs342863, rs368446, rs1194065

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

About this variant

This variant overlaps 5 transcripts and has 1094 individual genotypes.

Variation displays