Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3197832, rs17419810

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays