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rs786205617

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs786205617(-;-)
Make rs786205617(-;AA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66699067
GeneSPTBN2
is asnp
is mentioned by
dbSNPrs786205617
ebirs786205617
HLIrs786205617
Exacrs786205617
Varsomers786205617
Maprs786205617
PheGenIrs786205617
hapmaprs786205617
1000 genomesrs786205617
hgdprs786205617
ensemblrs786205617
gopubmedrs786205617
geneviewrs786205617
scholarrs786205617
googlers786205617
pharmgkbrs786205617
gwascentralrs786205617
openSNPrs786205617
23andMers786205617
23andMe allrs786205617
SNP Nexus

SNPshotrs786205617
SNPdbers786205617
MSV3drs786205617
GWAS Ctlgrs786205617
Max Magnitude0
ClinVar
Risk rs786205617(;)
Alt rs786205617(;)
Reference rs786205617(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTBN2
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66466538_66466539delTT
CLNSRC
CLNACC RCV000171463.1,