Original source

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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2511 sample genotypes.

Variant displays