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rs146075796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146075796(C;T)
Make rs146075796(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position39909834
GeneMOCS1
is asnp
is mentioned by
dbSNPrs146075796
dbSNP (old)rs146075796
ClinGenrs146075796
ebirs146075796
HLIrs146075796
Exacrs146075796
Gnomadrs146075796
Varsomers146075796
Maprs146075796
PheGenIrs146075796
Biobankrs146075796
1000 genomesrs146075796
hgdprs146075796
ensemblrs146075796
gopubmedrs146075796
geneviewrs146075796
scholarrs146075796
googlers146075796
pharmgkbrs146075796
gwascentralrs146075796
openSNPrs146075796
23andMers146075796
23andMe allrs146075796
SNPshotrs146075796
SNPdbers146075796
MSV3drs146075796
GWAS Ctlgrs146075796
Max Magnitude0
ClinVar
Risk rs146075796(T;T)
Alt rs146075796(T;T)
Reference Rs146075796(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MOCS1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.39877578C>T
CLNSRC
CLNACC RCV000254772.1,