Original source

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

T/- | Ancestral: T | MAF: 0.42 (-)

Chromosome 22:36353774 (forward strand) | View in location tab


with dbSNP rs369816888 (T/C)

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1095 individual genotypes.

Variation displays