Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome 1:91698441 (forward strand) | View in location tab

Co-located

with dbSNP rs202030205 (C/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71650462, rs57829068

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

Variation displays