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rs368775789

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368775789(C;T)
Make rs368775789(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position68935403
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs368775789
ebirs368775789
HLIrs368775789
Exacrs368775789
Varsomers368775789
Maprs368775789
PheGenIrs368775789
hapmaprs368775789
1000 genomesrs368775789
hgdprs368775789
ensemblrs368775789
gopubmedrs368775789
geneviewrs368775789
scholarrs368775789
googlers368775789
pharmgkbrs368775789
gwascentralrs368775789
openSNPrs368775789
23andMers368775789
23andMe allrs368775789
SNP Nexus

SNPshotrs368775789
SNPdbers368775789
MSV3drs368775789
GWAS Ctlgrs368775789
Max Magnitude0
ClinVar
Risk rs368775789(T;T)
Alt rs368775789(T;T)
Reference rs368775789(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IGHMBP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68702871C>A
CLNSRC
CLNACC RCV000236280.1,