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rs796052056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052056(-;GT)
Make rs796052056(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position73976399
GeneTMEM70
is asnp
is mentioned by
dbSNPrs796052056
dbSNP (old)rs796052056
ClinGenrs796052056
ebirs796052056
HLIrs796052056
Exacrs796052056
Gnomadrs796052056
Varsomers796052056
Maprs796052056
PheGenIrs796052056
Biobankrs796052056
1000 genomesrs796052056
hgdprs796052056
ensemblrs796052056
gopubmedrs796052056
geneviewrs796052056
scholarrs796052056
googlers796052056
pharmgkbrs796052056
gwascentralrs796052056
openSNPrs796052056
23andMers796052056
23andMe allrs796052056
SNP Nexus

SNPshotrs796052056
SNPdbers796052056
MSV3drs796052056
GWAS Ctlgrs796052056
Max Magnitude0
ClinVar
Risk rs796052056(GT;GT)
Alt rs796052056(GT;GT)
Reference Rs796052056(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TMEM70
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.74888633_74888634dupGT
CLNSRC
CLNACC RCV000186214.1,