Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.14 (G)
Location

Chromosome 7:155465199 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56669777, rs10356201

HGVS name

7:g.155465199A>G

This variation has assays on 9 chips - click the plus to show

Variation displays