Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064795665

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position66694147
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs1064795665
dbSNP (old)rs1064795665
ClinGenrs1064795665
ebirs1064795665
HLIrs1064795665
Exacrs1064795665
Gnomadrs1064795665
Varsomers1064795665
Maprs1064795665
PheGenIrs1064795665
Biobankrs1064795665
1000 genomesrs1064795665
hgdprs1064795665
ensemblrs1064795665
gopubmedrs1064795665
geneviewrs1064795665
scholarrs1064795665
googlers1064795665
pharmgkbrs1064795665
gwascentralrs1064795665
openSNPrs1064795665
23andMers1064795665
23andMe allrs1064795665
SNPshotrs1064795665
SNPdbers1064795665
MSV3drs1064795665
GWAS Ctlgrs1064795665
Max Magnitude0
ClinVar
Risk rs1064795665(C;C)
Alt rs1064795665(C;C)
Reference Rs1064795665(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTBN2
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66461618C>G
CLNSRC
CLNACC RCV000482504.1,