Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 19:50189876 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386603030, rs58503611

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

19:g.50189876T>C
ENST00000598205.4:c.-4+1569T>C

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

About this variant

This variant overlaps 1 transcript and has 3048 individual genotypes.

Variation displays