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rs786205585

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205585(C;G)
Make rs786205585(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5529307
GeneACTB
is asnp
is mentioned by
dbSNPrs786205585
ebirs786205585
HLIrs786205585
Exacrs786205585
Varsomers786205585
Maprs786205585
PheGenIrs786205585
hapmaprs786205585
1000 genomesrs786205585
hgdprs786205585
ensemblrs786205585
gopubmedrs786205585
geneviewrs786205585
scholarrs786205585
googlers786205585
pharmgkbrs786205585
gwascentralrs786205585
openSNPrs786205585
23andMers786205585
23andMe allrs786205585
SNP Nexus

SNPshotrs786205585
SNPdbers786205585
MSV3drs786205585
GWAS Ctlgrs786205585
Max Magnitude0
ClinVar
Risk rs786205585(G;G)
Alt rs786205585(G;G)
Reference rs786205585(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTB
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.5568938G>C
CLNSRC
CLNACC RCV000171405.1,