Original source

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

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

Chromosome 12:6537866 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Synonyms

Archive dbSNP rs3203505

This variant has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts and has 1 sample genotype.

Variant displays