Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.23 (C)
Location

Chromosome 22:40345340 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.40345340T>C

About this variant

This variant overlaps 10 transcripts and has 1097 individual genotypes.

Variation displays