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rs1064796568

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome5
Position177257097
GeneNSD1
is asnp
is mentioned by
dbSNPrs1064796568
dbSNP (old)rs1064796568
ClinGenrs1064796568
ebirs1064796568
HLIrs1064796568
Exacrs1064796568
Gnomadrs1064796568
Varsomers1064796568
Maprs1064796568
PheGenIrs1064796568
Biobankrs1064796568
1000 genomesrs1064796568
hgdprs1064796568
ensemblrs1064796568
gopubmedrs1064796568
geneviewrs1064796568
scholarrs1064796568
googlers1064796568
pharmgkbrs1064796568
gwascentralrs1064796568
openSNPrs1064796568
23andMers1064796568
23andMe allrs1064796568
SNPshotrs1064796568
SNPdbers1064796568
MSV3drs1064796568
GWAS Ctlgrs1064796568
Max Magnitude0
ClinVar
Risk rs1064796568(T;T)
Alt rs1064796568(T;T)
Reference Rs1064796568(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176684098C>T
CLNSRC
CLNACC RCV000485180.1,