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rs121909834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs121909834(-;T)
Make rs121909834(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position152869092
GeneNSDHL
is asnp
is mentioned by
dbSNPrs121909834
dbSNP (old)rs121909834
ClinGenrs121909834
ebirs121909834
HLIrs121909834
Exacrs121909834
Gnomadrs121909834
Varsomers121909834
Maprs121909834
PheGenIrs121909834
Biobankrs121909834
1000 genomesrs121909834
hgdprs121909834
ensemblrs121909834
gopubmedrs121909834
geneviewrs121909834
scholarrs121909834
googlers121909834
pharmgkbrs121909834
gwascentralrs121909834
openSNPrs121909834
23andMers121909834
23andMe allrs121909834
SNP Nexus

SNPshotrs121909834
SNPdbers121909834
MSV3drs121909834
GWAS Ctlgrs121909834
Max Magnitude0
OMIM300275
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909834(T;T)
Alt rs121909834(T;T)
Reference Rs121909834(-;-)
Significance Pathogenic
Disease NSDHL-Related Disorders
Variation info
Gene NSDHL
CLNDBN NSDHL-Related Disorders
Reversed 0
HGVS NC_000023.10:g.152037636dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000020428.11,