Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.49 (C)
Location

Chromosome 22:36800636 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

22:g.36800636C>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3690 sample genotypes.

Variant displays