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rs780594709

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780594709(C;T)
Make rs780594709(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position68933854
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs780594709
ebirs780594709
HLIrs780594709
Exacrs780594709
Varsomers780594709
Maprs780594709
PheGenIrs780594709
hapmaprs780594709
1000 genomesrs780594709
hgdprs780594709
ensemblrs780594709
gopubmedrs780594709
geneviewrs780594709
scholarrs780594709
googlers780594709
pharmgkbrs780594709
gwascentralrs780594709
openSNPrs780594709
23andMers780594709
23andMe allrs780594709
SNP Nexus

SNPshotrs780594709
SNPdbers780594709
MSV3drs780594709
GWAS Ctlgrs780594709
Max Magnitude0
ClinVar
Risk rs780594709(T;T)
Alt rs780594709(T;T)
Reference rs780594709(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IGHMBP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68701322C>T
CLNSRC
CLNACC RCV000223974.1,