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rs373730800

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs373730800(C;C)
Make rs373730800(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position66995320
GeneSBDS, TYW1
is asnp
is mentioned by
dbSNPrs373730800
ebirs373730800
HLIrs373730800
Exacrs373730800
Varsomers373730800
Maprs373730800
PheGenIrs373730800
hapmaprs373730800
1000 genomesrs373730800
hgdprs373730800
ensemblrs373730800
gopubmedrs373730800
geneviewrs373730800
scholarrs373730800
googlers373730800
pharmgkbrs373730800
gwascentralrs373730800
openSNPrs373730800
23andMers373730800
23andMe allrs373730800
SNP Nexus

SNPshotrs373730800
SNPdbers373730800
MSV3drs373730800
GWAS Ctlgrs373730800
Max Magnitude0
ClinVar
Risk rs373730800(C;C)
Alt rs373730800(C;C)
Reference rs373730800(T;T)
Significance Pathogenic
Disease Shwachman syndrome
Variation info
Gene SBDS TYW1
CLNDBN Shwachman syndrome
Reversed 0
HGVS NC_000007.13:g.66460307T>G
CLNSRC Baylor College of Medicine
CLNACC RCV000206645.1,