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rs387907028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907028(C;C)
Make rs387907028(C;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position968019
GeneRSPO4
is asnp
is mentioned by
dbSNPrs387907028
ebirs387907028
HLIrs387907028
Exacrs387907028
Varsomers387907028
Maprs387907028
PheGenIrs387907028
hapmaprs387907028
1000 genomesrs387907028
hgdprs387907028
ensemblrs387907028
gopubmedrs387907028
geneviewrs387907028
scholarrs387907028
googlers387907028
pharmgkbrs387907028
gwascentralrs387907028
openSNPrs387907028
23andMers387907028
23andMe allrs387907028
SNP Nexus

SNPshotrs387907028
SNPdbers387907028
MSV3drs387907028
GWAS Ctlgrs387907028
Max Magnitude0
ClinVar
Risk rs387907028(C;C)
Alt rs387907028(C;C)
Reference rs387907028(G;G)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.948662C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023832.2,