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rs886039603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039603(A;A)
Make rs886039603(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position46923222
GeneGOSR2
is asnp
is mentioned by
dbSNPrs886039603
dbSNP (classic)rs886039603
ClinGenrs886039603
ebirs886039603
HLIrs886039603
Exacrs886039603
Gnomadrs886039603
Varsomers886039603
LitVarrs886039603
Maprs886039603
PheGenIrs886039603
Biobankrs886039603
1000 genomesrs886039603
hgdprs886039603
ensemblrs886039603
geneviewrs886039603
scholarrs886039603
googlers886039603
pharmgkbrs886039603
gwascentralrs886039603
openSNPrs886039603
23andMers886039603
SNPshotrs886039603
SNPdbers886039603
MSV3drs886039603
GWAS Ctlgrs886039603
Max Magnitude0
ClinVar
Risk rs886039603(A;A)
Alt rs886039603(A;A)
Reference Rs886039603(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GOSR2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.45000588G>A
CLNSRC
CLNACC RCV000255066.1,