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rs765849229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765849229(A;A)
Make rs765849229(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position90791195
GeneADGRV1
is asnp
is mentioned by
dbSNPrs765849229
dbSNP (classic)rs765849229
ClinGenrs765849229
ebirs765849229
HLIrs765849229
Exacrs765849229
Gnomadrs765849229
Varsomers765849229
LitVarrs765849229
Maprs765849229
PheGenIrs765849229
Biobankrs765849229
1000 genomesrs765849229
hgdprs765849229
ensemblrs765849229
geneviewrs765849229
scholarrs765849229
googlers765849229
pharmgkbrs765849229
gwascentralrs765849229
openSNPrs765849229
23andMers765849229
SNPshotrs765849229
SNPdbers765849229
MSV3drs765849229
GWAS Ctlgrs765849229
Max Magnitude0
ClinVar
Risk rs765849229(A;A)
Alt rs765849229(A;A)
Reference Rs765849229(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GPR98 ADGRV1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.90087012G>A
CLNSRC
CLNACC RCV000482131.1,