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rs1064795719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position232531540
GeneCHRND
is asnp
is mentioned by
dbSNPrs1064795719
dbSNP (classic)rs1064795719
ClinGenrs1064795719
ebirs1064795719
HLIrs1064795719
Exacrs1064795719
Gnomadrs1064795719
Varsomers1064795719
LitVarrs1064795719
Maprs1064795719
PheGenIrs1064795719
Biobankrs1064795719
1000 genomesrs1064795719
hgdprs1064795719
ensemblrs1064795719
geneviewrs1064795719
scholarrs1064795719
googlers1064795719
pharmgkbrs1064795719
gwascentralrs1064795719
openSNPrs1064795719
23andMers1064795719
23andMe allrs1064795719
SNPshotrs1064795719
SNPdbers1064795719
MSV3drs1064795719
GWAS Ctlgrs1064795719
Max Magnitude0
ClinVar
Risk rs1064795719(G;G)
Alt rs1064795719(G;G)
Reference Rs1064795719(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHRND
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.233396250A>G
CLNSRC
CLNACC RCV000482356.1,