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rs786204766

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204766(A;A)
Make rs786204766(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position64794466
GeneSPTB
is asnp
is mentioned by
dbSNPrs786204766
ebirs786204766
HLIrs786204766
Exacrs786204766
Varsomers786204766
Maprs786204766
PheGenIrs786204766
hapmaprs786204766
1000 genomesrs786204766
hgdprs786204766
ensemblrs786204766
gopubmedrs786204766
geneviewrs786204766
scholarrs786204766
googlers786204766
pharmgkbrs786204766
gwascentralrs786204766
openSNPrs786204766
23andMers786204766
23andMe allrs786204766
SNP Nexus

SNPshotrs786204766
SNPdbers786204766
MSV3drs786204766
GWAS Ctlgrs786204766
Max Magnitude0
ClinVar
Risk rs786204766(A;A)
Alt rs786204766(A;A)
Reference rs786204766(G;G)
Significance Probable-Pathogenic
Disease Spherocytosis type 2
Variation info
Gene SPTB
CLNDBN Spherocytosis type 2
Reversed 1
HGVS NC_000014.8:g.65261184C>T
CLNSRC
CLNACC RCV000169630.1,