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rs577173144

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs577173144(A;A)
Make rs577173144(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position95799275
GeneCEP57
is asnp
is mentioned by
dbSNPrs577173144
ebirs577173144
HLIrs577173144
Exacrs577173144
Varsomers577173144
Maprs577173144
PheGenIrs577173144
hapmaprs577173144
1000 genomesrs577173144
hgdprs577173144
ensemblrs577173144
gopubmedrs577173144
geneviewrs577173144
scholarrs577173144
googlers577173144
pharmgkbrs577173144
gwascentralrs577173144
openSNPrs577173144
23andMers577173144
23andMe allrs577173144
SNP Nexus

SNPshotrs577173144
SNPdbers577173144
MSV3drs577173144
GWAS Ctlgrs577173144
Max Magnitude0
ClinVar
Risk rs577173144(A;A)
Alt rs577173144(A;A)
Reference rs577173144(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP57
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.95532439G>C
CLNSRC
CLNACC RCV000171200.1,