Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 1:12165862 (forward strand) | View in location tab

Co-located

with dbSNP rs113368176 (-/CTGTATTAGGGCTGGCA)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17882725, rs36205947

HGVS name

1:g.12165862A>C

Variation displays