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rs74315421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs74315421(C;C)
Make rs74315421(C;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position967264
GeneRSPO4
is asnp
is mentioned by
dbSNPrs74315421
ebirs74315421
HLIrs74315421
Exacrs74315421
Varsomers74315421
Maprs74315421
PheGenIrs74315421
hapmaprs74315421
1000 genomesrs74315421
hgdprs74315421
ensemblrs74315421
gopubmedrs74315421
geneviewrs74315421
scholarrs74315421
googlers74315421
pharmgkbrs74315421
gwascentralrs74315421
openSNPrs74315421
23andMers74315421
23andMe allrs74315421
SNP Nexus

SNPshotrs74315421
SNPdbers74315421
MSV3drs74315421
GWAS Ctlgrs74315421
Max Magnitude0
OMIM610573
Desc
Variant0002
Relatedalso
ClinVar
Risk rs74315421(C;C)
Alt rs74315421(C;C)
Reference rs74315421(T;T)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.947907A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001250.2,