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rs796052055

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052055(C;T)
Make rs796052055(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position73981416
GeneTMEM70
is asnp
is mentioned by
dbSNPrs796052055
ebirs796052055
HLIrs796052055
Exacrs796052055
Varsomers796052055
Maprs796052055
PheGenIrs796052055
hapmaprs796052055
1000 genomesrs796052055
hgdprs796052055
ensemblrs796052055
gopubmedrs796052055
geneviewrs796052055
scholarrs796052055
googlers796052055
pharmgkbrs796052055
gwascentralrs796052055
openSNPrs796052055
23andMers796052055
23andMe allrs796052055
SNP Nexus

SNPshotrs796052055
SNPdbers796052055
MSV3drs796052055
GWAS Ctlgrs796052055
Max Magnitude0
ClinVar
Risk rs796052055(T;T)
Alt rs796052055(T;T)
Reference rs796052055(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM70
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.74893651C>T
CLNSRC
CLNACC RCV000186212.1,