Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.01 (A)
Location

Chromosome 19:11377110 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs318716, rs642644, rs397184

HGVS name

19:g.11377110C>A

This variation has assays on 5 chips - click the plus to show

Variation displays