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rs797045835

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045835(-;CATG)
Make rs797045835(CATG;CATG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position152869035
GeneNSDHL
is asnp
is mentioned by
dbSNPrs797045835
ClinGenrs797045835
ebirs797045835
HLIrs797045835
Exacrs797045835
Varsomers797045835
Maprs797045835
PheGenIrs797045835
hapmaprs797045835
1000 genomesrs797045835
hgdprs797045835
ensemblrs797045835
gopubmedrs797045835
geneviewrs797045835
scholarrs797045835
googlers797045835
pharmgkbrs797045835
gwascentralrs797045835
openSNPrs797045835
23andMers797045835
23andMe allrs797045835
SNP Nexus

SNPshotrs797045835
SNPdbers797045835
MSV3drs797045835
GWAS Ctlgrs797045835
Max Magnitude0
ClinVar
Risk rs797045835(CATG;CATG)
Alt rs797045835(CATG;CATG)
Reference Rs797045835(;)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152037576_152037579dupCATG
CLNSRC
CLNACC RCV000192617.1,