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rs786205529

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205529(A;A)
Make rs786205529(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position96290475
GeneSNRNP200
is asnp
is mentioned by
dbSNPrs786205529
ebirs786205529
HLIrs786205529
Exacrs786205529
Varsomers786205529
Maprs786205529
PheGenIrs786205529
hapmaprs786205529
1000 genomesrs786205529
hgdprs786205529
ensemblrs786205529
gopubmedrs786205529
geneviewrs786205529
scholarrs786205529
googlers786205529
pharmgkbrs786205529
gwascentralrs786205529
openSNPrs786205529
23andMers786205529
23andMe allrs786205529
SNP Nexus

SNPshotrs786205529
SNPdbers786205529
MSV3drs786205529
GWAS Ctlgrs786205529
Max Magnitude0
ClinVar
Risk rs786205529(A;A)
Alt rs786205529(A;A)
Reference rs786205529(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SNRNP200
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.96956213C>T
CLNSRC
CLNACC RCV000171298.1,