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rs137853863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853863(A;G)
Make rs137853863(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position152869040
GeneNSDHL
is asnp
is mentioned by
dbSNPrs137853863
ebirs137853863
HLIrs137853863
Exacrs137853863
Varsomers137853863
Maprs137853863
PheGenIrs137853863
hapmaprs137853863
1000 genomesrs137853863
hgdprs137853863
ensemblrs137853863
gopubmedrs137853863
geneviewrs137853863
scholarrs137853863
googlers137853863
pharmgkbrs137853863
gwascentralrs137853863
openSNPrs137853863
23andMers137853863
23andMe allrs137853863
SNP Nexus

SNPshotrs137853863
SNPdbers137853863
MSV3drs137853863
GWAS Ctlgrs137853863
Max Magnitude0
ClinVar
Risk rs137853863(C,G;C,G)
Alt rs137853863(C,G;C,G)
Reference rs137853863(A;A)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152037584A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020427.1,


OMIM308050
Desc
Variant
Relatedalso