Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 7:39016603 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.39016603G>C

Variation displays