Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 2:210298541 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs3197832, rs17419810

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays