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rs387907223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907223(G;G)
Make rs387907223(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2884129
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs387907223
ebirs387907223
HLIrs387907223
Exacrs387907223
Varsomers387907223
Maprs387907223
PheGenIrs387907223
hapmaprs387907223
1000 genomesrs387907223
hgdprs387907223
ensemblrs387907223
gopubmedrs387907223
geneviewrs387907223
scholarrs387907223
googlers387907223
pharmgkbrs387907223
gwascentralrs387907223
openSNPrs387907223
23andMers387907223
23andMe allrs387907223
SNP Nexus

SNPshotrs387907223
SNPdbers387907223
MSV3drs387907223
GWAS Ctlgrs387907223
Max Magnitude0
ClinVar
Risk rs387907223(G;G)
Alt rs387907223(G;G)
Reference rs387907223(T;T)
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.2905359A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029183.3,