Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 8:133877623 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3758115, rs61207978

HGVS name

8:g.133877623A>G

Variation displays