Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: < 0.01 (C)
Location

Chromosome 17:43115791 (forward strand)|View in location tab

Co-located variant

dbSNP rs273902790 (G/-)

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB U14680.1:c.81-12C>G

HGVS names

This variant has 25 HGVS names - Show

About this variant

This variant overlaps 23 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays