Original source

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

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

Chromosome 19:5831983 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs16993198, rs2879400

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2506 sample genotypes.

Variant displays