Original source

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

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

Chromosome 5:136034508 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386608147

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 4 transcripts and has 2780 sample genotypes.

Variant displays