Original source

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

C/A | Ambiguity code: M | MAF: 0.49 (C)

Chromosome 12:49265973 (forward strand) | View in location tab


with dbSNP rs200653150 (C/-)

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1099 individual genotypes.

Variation displays