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rs193303102

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193303102(C;T)
Make rs193303102(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position144400250
GeneNOBOX
is asnp
is mentioned by
dbSNPrs193303102
ebirs193303102
HLIrs193303102
Exacrs193303102
Varsomers193303102
Maprs193303102
PheGenIrs193303102
hapmaprs193303102
1000 genomesrs193303102
hgdprs193303102
ensemblrs193303102
gopubmedrs193303102
geneviewrs193303102
scholarrs193303102
googlers193303102
pharmgkbrs193303102
gwascentralrs193303102
openSNPrs193303102
23andMers193303102
23andMe allrs193303102
SNP Nexus

SNPshotrs193303102
SNPdbers193303102
MSV3drs193303102
GWAS Ctlgrs193303102
Max Magnitude0
ClinVar
Risk rs193303102(T;T)
Alt rs193303102(T;T)
Reference rs193303102(C;C)
Significance Pathogenic
Disease Premature ovarian failure 5
Variation info
Gene NOBOX
CLNDBN Premature ovarian failure 5
Reversed 1
HGVS NC_000007.13:g.144097343G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000154189.3,