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rs796051985

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs796051985(-;-)
Make rs796051985(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position183041640
GeneMCCC1
is asnp
is mentioned by
dbSNPrs796051985
ebirs796051985
HLIrs796051985
Exacrs796051985
Varsomers796051985
Maprs796051985
PheGenIrs796051985
hapmaprs796051985
1000 genomesrs796051985
hgdprs796051985
ensemblrs796051985
gopubmedrs796051985
geneviewrs796051985
scholarrs796051985
googlers796051985
pharmgkbrs796051985
gwascentralrs796051985
openSNPrs796051985
23andMers796051985
23andMe allrs796051985
SNP Nexus

SNPshotrs796051985
SNPdbers796051985
MSV3drs796051985
GWAS Ctlgrs796051985
Max Magnitude0
ClinVar
Risk rs796051985(;)
Alt rs796051985(;)
Reference rs796051985(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.182759428_182759429delCA
CLNSRC
CLNACC RCV000185993.1,