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

rs387906922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906922(A;A)
Make rs387906922(A;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position41756757
GeneRIPK4
is asnp
is mentioned by
dbSNPrs387906922
ebirs387906922
HLIrs387906922
Exacrs387906922
Varsomers387906922
Maprs387906922
PheGenIrs387906922
hapmaprs387906922
1000 genomesrs387906922
hgdprs387906922
ensemblrs387906922
gopubmedrs387906922
geneviewrs387906922
scholarrs387906922
googlers387906922
pharmgkbrs387906922
gwascentralrs387906922
openSNPrs387906922
23andMers387906922
23andMe allrs387906922
SNP Nexus

SNPshotrs387906922
SNPdbers387906922
MSV3drs387906922
GWAS Ctlgrs387906922
Max Magnitude0
ClinVar
Risk rs387906922(A;A)
Alt rs387906922(A;A)
Reference rs387906922(T;T)
Significance Pathogenic
Disease Popliteal pterygium syndrome lethal type
Variation info
Gene RIPK4
CLNDBN Popliteal pterygium syndrome lethal type
Reversed 1
HGVS NC_000021.8:g.43176917A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023469.2,