Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 1:77554453 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60962074, rs74225868

HGVS name

1:g.77554453G>A

Variation displays