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rs137852855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852855(A;G)
Make rs137852855(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position4467245
GeneSUMF1
is asnp
is mentioned by
dbSNPrs137852855
ebirs137852855
HLIrs137852855
Exacrs137852855
Varsomers137852855
Maprs137852855
PheGenIrs137852855
hapmaprs137852855
1000 genomesrs137852855
hgdprs137852855
ensemblrs137852855
gopubmedrs137852855
geneviewrs137852855
scholarrs137852855
googlers137852855
pharmgkbrs137852855
gwascentralrs137852855
openSNPrs137852855
23andMers137852855
23andMe allrs137852855
SNP Nexus

SNPshotrs137852855
SNPdbers137852855
MSV3drs137852855
GWAS Ctlgrs137852855
Max Magnitude0
OMIM607939
Desc
Variant0017
Relatedalso
ClinVar
Risk rs137852855(G;G)
Alt rs137852855(G;G)
Reference rs137852855(A;A)
Significance Pathogenic
Disease Multiple sulfatase deficiency
Variation info
Gene SUMF1
CLNDBN Multiple sulfatase deficiency
Reversed 1
HGVS NC_000003.11:g.4508929T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002798.3,