Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 7:101127006 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36228266

HGVS name

7:g.101127006G>A

Variation displays