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rs786205545

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205545(C;C)
Make rs786205545(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position181558574
GeneCERKL
is asnp
is mentioned by
dbSNPrs786205545
ebirs786205545
HLIrs786205545
Exacrs786205545
Varsomers786205545
Maprs786205545
PheGenIrs786205545
hapmaprs786205545
1000 genomesrs786205545
hgdprs786205545
ensemblrs786205545
gopubmedrs786205545
geneviewrs786205545
scholarrs786205545
googlers786205545
pharmgkbrs786205545
gwascentralrs786205545
openSNPrs786205545
23andMers786205545
23andMe allrs786205545
SNP Nexus

SNPshotrs786205545
SNPdbers786205545
MSV3drs786205545
GWAS Ctlgrs786205545
Max Magnitude0
ClinVar
Risk rs786205545(C;C)
Alt rs786205545(C;C)
Reference rs786205545(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CERKL
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.182423301A>G
CLNSRC
CLNACC RCV000171327.1,