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rs587777303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777303(C;C)
Make rs587777303(C;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position166165800
GeneT
is asnp
is mentioned by
dbSNPrs587777303
ebirs587777303
HLIrs587777303
Exacrs587777303
Varsomers587777303
Maprs587777303
PheGenIrs587777303
hapmaprs587777303
1000 genomesrs587777303
hgdprs587777303
ensemblrs587777303
gopubmedrs587777303
geneviewrs587777303
scholarrs587777303
googlers587777303
pharmgkbrs587777303
gwascentralrs587777303
openSNPrs587777303
23andMers587777303
23andMe allrs587777303
SNP Nexus

SNPshotrs587777303
SNPdbers587777303
MSV3drs587777303
GWAS Ctlgrs587777303
Max Magnitude0
ClinVar
Risk rs587777303(C,T;C,T)
Alt rs587777303(C,T;C,T)
Reference rs587777303(A;A)
Significance Pathogenic
Disease Sacral agenesis with vertebral anomalies
Variation info
Gene T
CLNDBN Sacral agenesis with vertebral anomalies
Reversed 1
HGVS NC_000006.11:g.166579288T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000114433.3,