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rs760378316

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs760378316(A;A)
Make rs760378316(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position99203201
GeneKPNA7
is asnp
is mentioned by
dbSNPrs760378316
ebirs760378316
HLIrs760378316
Exacrs760378316
Varsomers760378316
Maprs760378316
PheGenIrs760378316
hapmaprs760378316
1000 genomesrs760378316
hgdprs760378316
ensemblrs760378316
gopubmedrs760378316
geneviewrs760378316
scholarrs760378316
googlers760378316
pharmgkbrs760378316
gwascentralrs760378316
openSNPrs760378316
23andMers760378316
23andMe allrs760378316
SNP Nexus

SNPshotrs760378316
SNPdbers760378316
MSV3drs760378316
GWAS Ctlgrs760378316
Max Magnitude0
ClinVar
Risk rs760378316(A;A)
Alt rs760378316(A;A)
Reference rs760378316(G;G)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene KPNA7
CLNDBN Intellectual disability, mild
Reversed 0
HGVS NC_000007.13:g.98800824G>A
CLNSRC Baylor College of Medicine
CLNACC RCV000191102.1,