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rs537043237

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs537043237(C;T)
Make rs537043237(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95606856
GeneALDH18A1
is asnp
is mentioned by
dbSNPrs537043237
ebirs537043237
HLIrs537043237
Exacrs537043237
Varsomers537043237
Maprs537043237
PheGenIrs537043237
hapmaprs537043237
1000 genomesrs537043237
hgdprs537043237
ensemblrs537043237
gopubmedrs537043237
geneviewrs537043237
scholarrs537043237
googlers537043237
pharmgkbrs537043237
gwascentralrs537043237
openSNPrs537043237
23andMers537043237
23andMe allrs537043237
SNP Nexus

SNPshotrs537043237
SNPdbers537043237
MSV3drs537043237
GWAS Ctlgrs537043237
Max Magnitude0
ClinVar
Risk rs537043237(T;T)
Alt rs537043237(T;T)
Reference rs537043237(C;C)
Significance Probable-Pathogenic
Disease Cutis laxa-corneal clouding-oligophrenia syndrome
Variation info
Gene ALDH18A1
CLNDBN Cutis laxa-corneal clouding-oligophrenia syndrome
Reversed 0
HGVS NC_000010.10:g.97366613C>T
CLNSRC
CLNACC RCV000196978.1,