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rs786205592

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205592(C;G)
Make rs786205592(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93780617
GeneTMEM67
is asnp
is mentioned by
dbSNPrs786205592
ebirs786205592
HLIrs786205592
Exacrs786205592
Varsomers786205592
Maprs786205592
PheGenIrs786205592
hapmaprs786205592
1000 genomesrs786205592
hgdprs786205592
ensemblrs786205592
gopubmedrs786205592
geneviewrs786205592
scholarrs786205592
googlers786205592
pharmgkbrs786205592
gwascentralrs786205592
openSNPrs786205592
23andMers786205592
23andMe allrs786205592
SNP Nexus

SNPshotrs786205592
SNPdbers786205592
MSV3drs786205592
GWAS Ctlgrs786205592
Max Magnitude0
ClinVar
Risk rs786205592(G;G)
Alt rs786205592(G;G)
Reference rs786205592(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM67
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.94792845C>G
CLNSRC
CLNACC RCV000171417.1,