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rs41298896

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41298896(C;C)
Make rs41298896(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position14926856
GeneDCLRE1C
is asnp
is mentioned by
dbSNPrs41298896
ebirs41298896
HLIrs41298896
Exacrs41298896
Varsomers41298896
Maprs41298896
PheGenIrs41298896
hapmaprs41298896
1000 genomesrs41298896
hgdprs41298896
ensemblrs41298896
gopubmedrs41298896
geneviewrs41298896
scholarrs41298896
googlers41298896
pharmgkbrs41298896
gwascentralrs41298896
openSNPrs41298896
23andMers41298896
23andMe allrs41298896
SNP Nexus

SNPshotrs41298896
SNPdbers41298896
MSV3drs41298896
GWAS Ctlgrs41298896
Max Magnitude0
ClinVar
Risk rs41298896(C;C)
Alt rs41298896(C;C)
Reference rs41298896(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene DCLRE1C
CLNDBN not provided not specified
Reversed 0
HGVS NC_000010.10:g.14968855G>C
CLNSRC
CLNACC RCV000124664.3, RCV000212484.1,