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rs768785753

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768785753(C;T)
Make rs768785753(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position183039072
GeneMCCC1
is asnp
is mentioned by
dbSNPrs768785753
ebirs768785753
HLIrs768785753
Exacrs768785753
Varsomers768785753
Maprs768785753
PheGenIrs768785753
hapmaprs768785753
1000 genomesrs768785753
hgdprs768785753
ensemblrs768785753
gopubmedrs768785753
geneviewrs768785753
scholarrs768785753
googlers768785753
pharmgkbrs768785753
gwascentralrs768785753
openSNPrs768785753
23andMers768785753
23andMe allrs768785753
SNP Nexus

SNPshotrs768785753
SNPdbers768785753
MSV3drs768785753
GWAS Ctlgrs768785753
Max Magnitude0
ClinVar
Risk rs768785753(T;T)
Alt rs768785753(T;T)
Reference rs768785753(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.182756860C>T
CLNSRC
CLNACC RCV000185991.1,