Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.39 (T)
Location

Chromosome 19:16123378 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3786570, rs58237666

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2511 sample genotypes.

Variant displays