Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (T)
Location

Chromosome 19:41758692 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3795019

This variation has 4 HGVS names - click the plus to show

19:g.41758692C>T
ENST00000601409.1:n.384-611G>A
ENST00000598976.1:c.425-2557C>T
ENST00000199764.6:c.424+1733C>T

Variation displays