Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.17 (C)
Location

Chromosome 6:136999730 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs1775299, rs58994219

HGVS name

6:g.136999730C>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 5 transcripts and has 3509 sample genotypes.

Variant displays