Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: < 0.01 (C)
Location

Chromosome 19:840713 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs597148

HGVS name

19:g.840713G>C

About this variant

This variant overlaps 2 transcripts and has 2540 sample genotypes.

Variant displays