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rs387907027

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907027(C;T)
Make rs387907027(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position968028
GeneRSPO4
is asnp
is mentioned by
dbSNPrs387907027
ebirs387907027
HLIrs387907027
Exacrs387907027
Varsomers387907027
Maprs387907027
PheGenIrs387907027
hapmaprs387907027
1000 genomesrs387907027
hgdprs387907027
ensemblrs387907027
gopubmedrs387907027
geneviewrs387907027
scholarrs387907027
googlers387907027
pharmgkbrs387907027
gwascentralrs387907027
openSNPrs387907027
23andMers387907027
23andMe allrs387907027
SNP Nexus

SNPshotrs387907027
SNPdbers387907027
MSV3drs387907027
GWAS Ctlgrs387907027
Max Magnitude0
ClinVar
Risk rs387907027(T;T)
Alt rs387907027(T;T)
Reference rs387907027(C;C)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.948671G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023831.2,