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rs193303103

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193303103(C;C)
Make rs193303103(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position144400132
GeneNOBOX
is asnp
is mentioned by
dbSNPrs193303103
ebirs193303103
HLIrs193303103
Exacrs193303103
Varsomers193303103
Maprs193303103
PheGenIrs193303103
hapmaprs193303103
1000 genomesrs193303103
hgdprs193303103
ensemblrs193303103
gopubmedrs193303103
geneviewrs193303103
scholarrs193303103
googlers193303103
pharmgkbrs193303103
gwascentralrs193303103
openSNPrs193303103
23andMers193303103
23andMe allrs193303103
SNP Nexus

SNPshotrs193303103
SNPdbers193303103
MSV3drs193303103
GWAS Ctlgrs193303103
Max Magnitude0
ClinVar
Risk rs193303103(C;C)
Alt rs193303103(C;C)
Reference rs193303103(G;G)
Significance Pathogenic
Disease Premature ovarian failure 5
Variation info
Gene NOBOX
CLNDBN Premature ovarian failure 5
Reversed 1
HGVS NC_000007.13:g.144097225C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000154192.3,