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rs796051984

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051984(C;T)
Make rs796051984(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position183072477
GeneMCCC1
is asnp
is mentioned by
dbSNPrs796051984
ebirs796051984
HLIrs796051984
Exacrs796051984
Varsomers796051984
Maprs796051984
PheGenIrs796051984
hapmaprs796051984
1000 genomesrs796051984
hgdprs796051984
ensemblrs796051984
gopubmedrs796051984
geneviewrs796051984
scholarrs796051984
googlers796051984
pharmgkbrs796051984
gwascentralrs796051984
openSNPrs796051984
23andMers796051984
23andMe allrs796051984
SNP Nexus

SNPshotrs796051984
SNPdbers796051984
MSV3drs796051984
GWAS Ctlgrs796051984
Max Magnitude0
ClinVar
Risk rs796051984(T;T)
Alt rs796051984(T;T)
Reference rs796051984(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.182790265G>A
CLNSRC
CLNACC RCV000185988.1,