Original source

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

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

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

Co-located

with dbSNP rs66795691 (ATA/CTC)

Most severe consequence
Evidence status

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

Variation displays