Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.30 (T)
Location

Chromosome 9:35080833 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, has 2599 sample genotypes and is mentioned in 1 citation.

Variant displays