Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.49 (G)
Location

Chromosome 19:42322547 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59430921, rs74259553

HGVS name

19:g.42322547G>A

This variation has assays on 6 chips - click the plus to show

Variation displays