Original source

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

C/A | Ambiguity code: M | MAF: 0.41 (A)

Chromosome 7:76416816 (forward strand) | View in location tab


with dbSNP rs66795691 (ATA/CTC)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 1 transcript and has 1099 individual genotypes.

Variation displays