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rs201088712

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201088712(C;G)
Make rs201088712(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position24906775
GeneCENPJ
is asnp
is mentioned by
dbSNPrs201088712
ebirs201088712
HLIrs201088712
Exacrs201088712
Varsomers201088712
Maprs201088712
PheGenIrs201088712
hapmaprs201088712
1000 genomesrs201088712
hgdprs201088712
ensemblrs201088712
gopubmedrs201088712
geneviewrs201088712
scholarrs201088712
googlers201088712
pharmgkbrs201088712
gwascentralrs201088712
openSNPrs201088712
23andMers201088712
23andMe allrs201088712
SNP Nexus

SNPshotrs201088712
SNPdbers201088712
MSV3drs201088712
GWAS Ctlgrs201088712
Max Magnitude0
ClinVar
Risk rs201088712(G;G)
Alt rs201088712(G;G)
Reference rs201088712(C;C)
Significance Probable-Pathogenic
Disease Seckel syndrome 4
Variation info
Gene CENPJ
CLNDBN Seckel syndrome 4
Reversed 0
HGVS NC_000013.10:g.25480913C>G
CLNSRC
CLNACC RCV000194381.1,