Original source

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

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

Chromosome 4:123395529 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs301332, rs59921662

HGVS name

4:g.123395529A>G

This variation has assays on 4 chips - click the plus to show

Variation displays