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: 0.44 (A)
Location

Chromosome 19:45937042 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59992602, rs17652042

This variation has 2 HGVS names - click the plus to show

19:g.45937042A>G
ENST00000263257.5:c.*2821T>C

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

Variation displays