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rs141571609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141571609(A;A)
Make rs141571609(A;C)
ReferenceGRCh38 38.1/142
ChromosomeX
Position152867641
GeneNSDHL
is asnp
is mentioned by
dbSNPrs141571609
ebirs141571609
HLIrs141571609
Exacrs141571609
Varsomers141571609
Maprs141571609
PheGenIrs141571609
hapmaprs141571609
1000 genomesrs141571609
hgdprs141571609
ensemblrs141571609
gopubmedrs141571609
geneviewrs141571609
scholarrs141571609
googlers141571609
pharmgkbrs141571609
gwascentralrs141571609
openSNPrs141571609
23andMers141571609
23andMe allrs141571609
SNP Nexus

SNPshotrs141571609
SNPdbers141571609
MSV3drs141571609
GWAS Ctlgrs141571609
Max Magnitude0
ClinVar
Risk rs141571609(A,T;A,T)
Alt rs141571609(A,T;A,T)
Reference rs141571609(C;C)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152036185C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000146965.1,