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rs387907226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907226(A;G)
Make rs387907226(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2884123
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs387907226
ebirs387907226
HLIrs387907226
Exacrs387907226
Varsomers387907226
Maprs387907226
PheGenIrs387907226
hapmaprs387907226
1000 genomesrs387907226
hgdprs387907226
ensemblrs387907226
gopubmedrs387907226
geneviewrs387907226
scholarrs387907226
googlers387907226
pharmgkbrs387907226
gwascentralrs387907226
openSNPrs387907226
23andMers387907226
23andMe allrs387907226
SNP Nexus

SNPshotrs387907226
SNPdbers387907226
MSV3drs387907226
GWAS Ctlgrs387907226
Max Magnitude0
ClinVar
Risk rs387907226(G;G)
Alt rs387907226(G;G)
Reference rs387907226(A;A)
Significance Pathogenic
Disease Intrauterine growth retardation
Variation info
Gene CDKN1C
CLNDBN Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
Reversed 1
HGVS NC_000011.9:g.2905353T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029187.4,