Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 19:19358820 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61503628, rs386509244

HGVS name

19:g.19358820T>C

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays