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rs74315422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315422(A;A)
Make rs74315422(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position967230
GeneRSPO4
is asnp
is mentioned by
dbSNPrs74315422
ebirs74315422
HLIrs74315422
Exacrs74315422
Varsomers74315422
Maprs74315422
PheGenIrs74315422
hapmaprs74315422
1000 genomesrs74315422
hgdprs74315422
ensemblrs74315422
gopubmedrs74315422
geneviewrs74315422
scholarrs74315422
googlers74315422
pharmgkbrs74315422
gwascentralrs74315422
openSNPrs74315422
23andMers74315422
23andMe allrs74315422
SNP Nexus

SNPshotrs74315422
SNPdbers74315422
MSV3drs74315422
GWAS Ctlgrs74315422
Max Magnitude0
OMIM610573
Desc
Variant0003
Relatedalso
ClinVar
Risk rs74315422(A;A)
Alt rs74315422(A;A)
Reference rs74315422(G;G)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.947873C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001251.2,