Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: < 0.01 (C)
Location

Chromosome 16:22205270 (forward strand)|View in location tab

Co-located variant

dbSNP rs757293640 (A/-)

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.22205270A>C

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays