Original source

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

C/A/G | Ancestral: G | Ambiguity code: V | MAF: 0.19 (A)

Chromosome 17:63919146 (forward strand) | View in location tab


with dbSNP rs41299069 (G/T)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts and has 1094 individual genotypes.

Variation displays