Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.02 (C)
Location

Chromosome 19:45415362 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2505 sample genotypes.

Variant displays