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rs886039893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039893(G;T)
Make rs886039893(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position90694362
GeneADGRV1
is asnp
is mentioned by
dbSNPrs886039893
dbSNP (classic)rs886039893
ClinGenrs886039893
ebirs886039893
HLIrs886039893
Exacrs886039893
Gnomadrs886039893
Varsomers886039893
LitVarrs886039893
Maprs886039893
PheGenIrs886039893
Biobankrs886039893
1000 genomesrs886039893
hgdprs886039893
ensemblrs886039893
geneviewrs886039893
scholarrs886039893
googlers886039893
pharmgkbrs886039893
gwascentralrs886039893
openSNPrs886039893
23andMers886039893
SNPshotrs886039893
SNPdbers886039893
MSV3drs886039893
GWAS Ctlgrs886039893
Max Magnitude0
ClinVar
Risk rs886039893(T;T)
Alt rs886039893(T;T)
Reference Rs886039893(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89990179G>T
CLNSRC
CLNACC RCV000256377.1,