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rs200820631

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200820631(C;T)
Make rs200820631(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position73981293
GeneTMEM70
is asnp
is mentioned by
dbSNPrs200820631
ebirs200820631
HLIrs200820631
Exacrs200820631
Varsomers200820631
Maprs200820631
PheGenIrs200820631
hapmaprs200820631
1000 genomesrs200820631
hgdprs200820631
ensemblrs200820631
gopubmedrs200820631
geneviewrs200820631
scholarrs200820631
googlers200820631
pharmgkbrs200820631
gwascentralrs200820631
openSNPrs200820631
23andMers200820631
23andMe allrs200820631
SNP Nexus

SNPshotrs200820631
SNPdbers200820631
MSV3drs200820631
GWAS Ctlgrs200820631
Max Magnitude0
ClinVar
Risk rs200820631(T;T)
Alt rs200820631(T;T)
Reference rs200820631(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM70
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.74893528C>T
CLNSRC
CLNACC RCV000186210.1,