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rs797045448

From SNPedia

Orientationminus
Make rs797045448(-;-)
Make rs797045448(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position24906187
GeneCENPJ
is asnp
is mentioned by
dbSNPrs797045448
ebirs797045448
HLIrs797045448
Exacrs797045448
Varsomers797045448
Maprs797045448
PheGenIrs797045448
hapmaprs797045448
1000 genomesrs797045448
hgdprs797045448
ensemblrs797045448
gopubmedrs797045448
geneviewrs797045448
scholarrs797045448
googlers797045448
pharmgkbrs797045448
gwascentralrs797045448
openSNPrs797045448
23andMers797045448
23andMe allrs797045448
SNP Nexus

SNPshotrs797045448
SNPdbers797045448
MSV3drs797045448
GWAS Ctlgrs797045448
Max Magnitude
ClinVar
Risk rs797045448(;)
Alt rs797045448(;)
Reference rs797045448(CT;CT)
Significance Pathogenic
Disease Seckel syndrome 4
Variation info
Gene CENPJ
CLNDBN Seckel syndrome 4
Reversed 1
HGVS NC_000013.10:g.25480325_25480326delAG
CLNSRC
CLNACC RCV000192528.1,