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rs768138495

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs768138495(-;-)
Make rs768138495(-;C)
Make rs768138495(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position968119
GeneRSPO4
is asnp
is mentioned by
dbSNPrs768138495
ebirs768138495
HLIrs768138495
Exacrs768138495
Varsomers768138495
Maprs768138495
PheGenIrs768138495
hapmaprs768138495
1000 genomesrs768138495
hgdprs768138495
ensemblrs768138495
gopubmedrs768138495
geneviewrs768138495
scholarrs768138495
googlers768138495
pharmgkbrs768138495
gwascentralrs768138495
openSNPrs768138495
23andMers768138495
23andMe allrs768138495
SNP Nexus

SNPshotrs768138495
SNPdbers768138495
MSV3drs768138495
GWAS Ctlgrs768138495
Max Magnitude0
ClinVar
Risk rs768138495(C;C)
Alt rs768138495(C;C)
Reference rs768138495(;)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 0
HGVS NC_000020.10:g.948763dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001253.4,