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rs1064795088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position47181405
GeneRBM10
is asnp
is mentioned by
dbSNPrs1064795088
dbSNP (old)rs1064795088
ClinGenrs1064795088
ebirs1064795088
HLIrs1064795088
Exacrs1064795088
Gnomadrs1064795088
Varsomers1064795088
Maprs1064795088
PheGenIrs1064795088
Biobankrs1064795088
1000 genomesrs1064795088
hgdprs1064795088
ensemblrs1064795088
gopubmedrs1064795088
geneviewrs1064795088
scholarrs1064795088
googlers1064795088
pharmgkbrs1064795088
gwascentralrs1064795088
openSNPrs1064795088
23andMers1064795088
23andMe allrs1064795088
SNPshotrs1064795088
SNPdbers1064795088
MSV3drs1064795088
GWAS Ctlgrs1064795088
Max Magnitude0
ClinVar
Risk rs1064795088(-;-)
Alt rs1064795088(-;-)
Reference Rs1064795088(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RBM10
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.47040804delA
CLNSRC
CLNACC RCV000479448.1,