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rs758719615

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758719615(G;T)
Make rs758719615(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74743905
GeneKIAA2022
is asnp
is mentioned by
dbSNPrs758719615
ebirs758719615
HLIrs758719615
Exacrs758719615
Varsomers758719615
Maprs758719615
PheGenIrs758719615
hapmaprs758719615
1000 genomesrs758719615
hgdprs758719615
ensemblrs758719615
gopubmedrs758719615
geneviewrs758719615
scholarrs758719615
googlers758719615
pharmgkbrs758719615
gwascentralrs758719615
openSNPrs758719615
23andMers758719615
23andMe allrs758719615
SNP Nexus

SNPshotrs758719615
SNPdbers758719615
MSV3drs758719615
GWAS Ctlgrs758719615
Max Magnitude0
ClinVar
Risk rs758719615(T;T)
Alt rs758719615(T;T)
Reference rs758719615(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KIAA2022
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.73963740G>A
CLNSRC
CLNACC RCV000233744.1,