Original source

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

T/C | Ancestral: C | Ambiguity code: Y

Chromosome 19:5831875 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs3896735

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 1 sample genotype.

Variant displays