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rs796051987

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051987(C;C)
Make rs796051987(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position183092521
GeneMCCC1
is asnp
is mentioned by
dbSNPrs796051987
ebirs796051987
HLIrs796051987
Exacrs796051987
Varsomers796051987
Maprs796051987
PheGenIrs796051987
hapmaprs796051987
1000 genomesrs796051987
hgdprs796051987
ensemblrs796051987
gopubmedrs796051987
geneviewrs796051987
scholarrs796051987
googlers796051987
pharmgkbrs796051987
gwascentralrs796051987
openSNPrs796051987
23andMers796051987
23andMe allrs796051987
SNP Nexus

SNPshotrs796051987
SNPdbers796051987
MSV3drs796051987
GWAS Ctlgrs796051987
Max Magnitude0
ClinVar
Risk rs796051987(C;C)
Alt rs796051987(C;C)
Reference rs796051987(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.182810309A>G
CLNSRC
CLNACC RCV000185996.1,