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rs1064795587

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position3659949
GeneCTNS, LOC105371492
is asnp
is mentioned by
dbSNPrs1064795587
dbSNP (old)rs1064795587
ClinGenrs1064795587
ebirs1064795587
HLIrs1064795587
Exacrs1064795587
Gnomadrs1064795587
Varsomers1064795587
Maprs1064795587
PheGenIrs1064795587
Biobankrs1064795587
1000 genomesrs1064795587
hgdprs1064795587
ensemblrs1064795587
gopubmedrs1064795587
geneviewrs1064795587
scholarrs1064795587
googlers1064795587
pharmgkbrs1064795587
gwascentralrs1064795587
openSNPrs1064795587
23andMers1064795587
23andMe allrs1064795587
SNPshotrs1064795587
SNPdbers1064795587
MSV3drs1064795587
GWAS Ctlgrs1064795587
Max Magnitude0
ClinVar
Risk rs1064795587(G;G)
Alt rs1064795587(G;G)
Reference Rs1064795587(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTNS
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.3563243A>G
CLNSRC
CLNACC RCV000479734.1,