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rs796051986

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051986(-;-)
Make rs796051986(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position183039040
GeneMCCC1
is asnp
is mentioned by
dbSNPrs796051986
ebirs796051986
HLIrs796051986
Exacrs796051986
Varsomers796051986
Maprs796051986
PheGenIrs796051986
hapmaprs796051986
1000 genomesrs796051986
hgdprs796051986
ensemblrs796051986
gopubmedrs796051986
geneviewrs796051986
scholarrs796051986
googlers796051986
pharmgkbrs796051986
gwascentralrs796051986
openSNPrs796051986
23andMers796051986
23andMe allrs796051986
SNP Nexus

SNPshotrs796051986
SNPdbers796051986
MSV3drs796051986
GWAS Ctlgrs796051986
Max Magnitude0
ClinVar
Risk rs796051986(;)
Alt rs796051986(;)
Reference rs796051986(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.182756828delG
CLNSRC
CLNACC RCV000185994.1,