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rs786205134

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205134(A;A)
Make rs786205134(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position111840653
GeneALG9
is asnp
is mentioned by
dbSNPrs786205134
ebirs786205134
HLIrs786205134
Exacrs786205134
Varsomers786205134
Maprs786205134
PheGenIrs786205134
hapmaprs786205134
1000 genomesrs786205134
hgdprs786205134
ensemblrs786205134
gopubmedrs786205134
geneviewrs786205134
scholarrs786205134
googlers786205134
pharmgkbrs786205134
gwascentralrs786205134
openSNPrs786205134
23andMers786205134
23andMe allrs786205134
SNP Nexus

SNPshotrs786205134
SNPdbers786205134
MSV3drs786205134
GWAS Ctlgrs786205134
Max Magnitude0
ClinVar
Risk rs786205134(A;A)
Alt rs786205134(A;A)
Reference rs786205134(T;T)
Significance Pathogenic
Disease Gillessen-Kaesbach-Nishimura dysplasia Gillessen-kaesbach-nishimura syndrome
Variation info
Gene ALG9
CLNDBN Gillessen-Kaesbach-Nishimura dysplasia Gillessen-kaesbach-nishimura syndrome
Reversed 1
HGVS NC_000011.9:g.111711376A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170339.1, RCV000211586.1,