Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.02 (C)
Location

Chromosome 12:21635668 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs7297559, rs11547918

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 5 transcripts and has 3197 sample genotypes.

Variant displays