Have questions? Visit https://www.reddit.com/r/SNPedia

rs74315423

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315423(A;A)
Make rs74315423(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position968000
GeneRSPO4
is asnp
is mentioned by
dbSNPrs74315423
ebirs74315423
HLIrs74315423
Exacrs74315423
Varsomers74315423
Maprs74315423
PheGenIrs74315423
hapmaprs74315423
1000 genomesrs74315423
hgdprs74315423
ensemblrs74315423
gopubmedrs74315423
geneviewrs74315423
scholarrs74315423
googlers74315423
pharmgkbrs74315423
gwascentralrs74315423
openSNPrs74315423
23andMers74315423
23andMe allrs74315423
SNP Nexus

SNPshotrs74315423
SNPdbers74315423
MSV3drs74315423
GWAS Ctlgrs74315423
Max Magnitude0
OMIM610573
Desc
Variant0004
Relatedalso
ClinVar
Risk rs74315423(A;A)
Alt rs74315423(A;A)
Reference rs74315423(G;G)
Significance Pathogenic
Disease Anonychia
Variation info
Gene RSPO4
CLNDBN Anonychia
Reversed 1
HGVS NC_000020.10:g.948643C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001252.4,