Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.15 (A)
Location

Chromosome 19:5839613 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17748601, rs57750337

This variation has 5 HGVS names - click the plus to show

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

Variation displays