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rs765368797

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765368797(C;C)
Make rs765368797(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138570987
GeneHSPA9, LOC105379193
is asnp
is mentioned by
dbSNPrs765368797
ebirs765368797
HLIrs765368797
Exacrs765368797
Varsomers765368797
Maprs765368797
PheGenIrs765368797
hapmaprs765368797
1000 genomesrs765368797
hgdprs765368797
ensemblrs765368797
gopubmedrs765368797
geneviewrs765368797
scholarrs765368797
googlers765368797
pharmgkbrs765368797
gwascentralrs765368797
openSNPrs765368797
23andMers765368797
23andMe allrs765368797
SNP Nexus

SNPshotrs765368797
SNPdbers765368797
MSV3drs765368797
GWAS Ctlgrs765368797
Max Magnitude0
ClinVar
Risk rs765368797(C;C)
Alt rs765368797(C;C)
Reference rs765368797(T;T)
Significance Pathogenic
Disease Even-plus syndrome
Variation info
Gene HSPA9
CLNDBN Even-plus syndrome
Reversed 0
HGVS NC_000005.9:g.137906676T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000209966.2,