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rs1057518588

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518588(A;A)
Make rs1057518588(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position68908632
GeneIGHMBP2
is asnp
is mentioned by
dbSNPrs1057518588
dbSNP (old)rs1057518588
ClinGenrs1057518588
ebirs1057518588
HLIrs1057518588
Exacrs1057518588
Gnomadrs1057518588
Varsomers1057518588
Maprs1057518588
PheGenIrs1057518588
Biobankrs1057518588
1000 genomesrs1057518588
hgdprs1057518588
ensemblrs1057518588
gopubmedrs1057518588
geneviewrs1057518588
scholarrs1057518588
googlers1057518588
pharmgkbrs1057518588
gwascentralrs1057518588
openSNPrs1057518588
23andMers1057518588
23andMe allrs1057518588
SNPshotrs1057518588
SNPdbers1057518588
MSV3drs1057518588
GWAS Ctlgrs1057518588
Max Magnitude0
ClinVar
Risk rs1057518588(A;A)
Alt rs1057518588(A;A)
Reference Rs1057518588(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IGHMBP2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68676100G>A
CLNSRC
CLNACC RCV000412903.1,