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rs137853862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853862(A;A)
Make rs137853862(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position152858872
GeneNSDHL
is asnp
is mentioned by
dbSNPrs137853862
ebirs137853862
HLIrs137853862
Exacrs137853862
Varsomers137853862
Maprs137853862
PheGenIrs137853862
hapmaprs137853862
1000 genomesrs137853862
hgdprs137853862
ensemblrs137853862
gopubmedrs137853862
geneviewrs137853862
scholarrs137853862
googlers137853862
pharmgkbrs137853862
gwascentralrs137853862
openSNPrs137853862
23andMers137853862
23andMe allrs137853862
SNP Nexus

SNPshotrs137853862
SNPdbers137853862
MSV3drs137853862
GWAS Ctlgrs137853862
Max Magnitude0
ClinVar
Risk rs137853862(A;A)
Alt rs137853862(A;A)
Reference rs137853862(G;G)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152027416G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020429.1,


OMIM308050
Desc
Variant
Relatedalso