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rs201060167

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201060167(C;C)
Make rs201060167(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position68929204
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs201060167
ebirs201060167
HLIrs201060167
Exacrs201060167
Varsomers201060167
Maprs201060167
PheGenIrs201060167
hapmaprs201060167
1000 genomesrs201060167
hgdprs201060167
ensemblrs201060167
gopubmedrs201060167
geneviewrs201060167
scholarrs201060167
googlers201060167
pharmgkbrs201060167
gwascentralrs201060167
openSNPrs201060167
23andMers201060167
23andMe allrs201060167
SNP Nexus

SNPshotrs201060167
SNPdbers201060167
MSV3drs201060167
GWAS Ctlgrs201060167
Max Magnitude0
ClinVar
Risk rs201060167(C;C)
Alt rs201060167(C;C)
Reference rs201060167(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene IGHMBP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68696672T>C
CLNSRC
CLNACC RCV000236185.1,