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rs745973997

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs745973997(A;A)
Make rs745973997(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position2646435
GeneVLDLR
is asnp
is mentioned by
dbSNPrs745973997
dbSNP (classic)rs745973997
ClinGenrs745973997
ebirs745973997
HLIrs745973997
Exacrs745973997
Gnomadrs745973997
Varsomers745973997
LitVarrs745973997
Maprs745973997
PheGenIrs745973997
Biobankrs745973997
1000 genomesrs745973997
hgdprs745973997
ensemblrs745973997
geneviewrs745973997
scholarrs745973997
googlers745973997
pharmgkbrs745973997
gwascentralrs745973997
openSNPrs745973997
23andMers745973997
SNPshotrs745973997
SNPdbers745973997
MSV3drs745973997
GWAS Ctlgrs745973997
Max Magnitude0
ClinVar
Risk rs745973997(A;A)
Alt rs745973997(A;A)
Reference Rs745973997(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene VLDLR
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.2646435G>A
CLNSRC
CLNACC RCV000255297.1,