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

rs515726203

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726203(A;C)
Make rs515726203(C;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position2884675
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs515726203
ebirs515726203
HLIrs515726203
Exacrs515726203
Varsomers515726203
Maprs515726203
PheGenIrs515726203
hapmaprs515726203
1000 genomesrs515726203
hgdprs515726203
ensemblrs515726203
gopubmedrs515726203
geneviewrs515726203
scholarrs515726203
googlers515726203
pharmgkbrs515726203
gwascentralrs515726203
openSNPrs515726203
23andMers515726203
23andMe allrs515726203
SNP Nexus

SNPshotrs515726203
SNPdbers515726203
MSV3drs515726203
GWAS Ctlgrs515726203
Max Magnitude0
ClinVar
Risk rs515726203(C;C)
Alt rs515726203(C;C)
Reference rs515726203(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 0
HGVS NC_000011.9:g.2905905A>C
CLNSRC ClinVar
CLNACC RCV000119018.2,