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rs786205608

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205608(A;G)
Make rs786205608(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93787842
GeneTMEM67
is asnp
is mentioned by
dbSNPrs786205608
ebirs786205608
HLIrs786205608
Exacrs786205608
Varsomers786205608
Maprs786205608
PheGenIrs786205608
hapmaprs786205608
1000 genomesrs786205608
hgdprs786205608
ensemblrs786205608
gopubmedrs786205608
geneviewrs786205608
scholarrs786205608
googlers786205608
pharmgkbrs786205608
gwascentralrs786205608
openSNPrs786205608
23andMers786205608
23andMe allrs786205608
SNP Nexus

SNPshotrs786205608
SNPdbers786205608
MSV3drs786205608
GWAS Ctlgrs786205608
Max Magnitude0
ClinVar
Risk rs786205608(G;G)
Alt rs786205608(G;G)
Reference Rs786205608(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM67
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.94800070A>G
CLNSRC
CLNACC RCV000171449.1,