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rs763670293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763670293(C;T)
Make rs763670293(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position90728720
GeneADGRV1, LOC105379077
is asnp
is mentioned by
dbSNPrs763670293
dbSNP (classic)rs763670293
ClinGenrs763670293
ebirs763670293
HLIrs763670293
Exacrs763670293
Gnomadrs763670293
Varsomers763670293
LitVarrs763670293
Maprs763670293
PheGenIrs763670293
Biobankrs763670293
1000 genomesrs763670293
hgdprs763670293
ensemblrs763670293
geneviewrs763670293
scholarrs763670293
googlers763670293
pharmgkbrs763670293
gwascentralrs763670293
openSNPrs763670293
23andMers763670293
SNPshotrs763670293
SNPdbers763670293
MSV3drs763670293
GWAS Ctlgrs763670293
Max Magnitude0
ClinVar
Risk rs763670293(T;T)
Alt rs763670293(T;T)
Reference Rs763670293(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADGRV1 GPR98
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.90024537C>T
CLNSRC
CLNACC RCV000255292.1,