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rs786205547

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205547(C;C)
Make rs786205547(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position219157471
GeneNHEJ1
is asnp
is mentioned by
dbSNPrs786205547
ebirs786205547
HLIrs786205547
Exacrs786205547
Varsomers786205547
Maprs786205547
PheGenIrs786205547
hapmaprs786205547
1000 genomesrs786205547
hgdprs786205547
ensemblrs786205547
gopubmedrs786205547
geneviewrs786205547
scholarrs786205547
googlers786205547
pharmgkbrs786205547
gwascentralrs786205547
openSNPrs786205547
23andMers786205547
23andMe allrs786205547
SNP Nexus

SNPshotrs786205547
SNPdbers786205547
MSV3drs786205547
GWAS Ctlgrs786205547
Max Magnitude0
ClinVar
Risk rs786205547(C;C)
Alt rs786205547(C;C)
Reference rs786205547(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NHEJ1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.220022193C>G
CLNSRC
CLNACC RCV000171332.1,