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rs1064796690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome5
Position177280757
GeneNSD1
is asnp
is mentioned by
dbSNPrs1064796690
dbSNP (old)rs1064796690
ClinGenrs1064796690
ebirs1064796690
HLIrs1064796690
Exacrs1064796690
Gnomadrs1064796690
Varsomers1064796690
Maprs1064796690
PheGenIrs1064796690
Biobankrs1064796690
1000 genomesrs1064796690
hgdprs1064796690
ensemblrs1064796690
gopubmedrs1064796690
geneviewrs1064796690
scholarrs1064796690
googlers1064796690
pharmgkbrs1064796690
gwascentralrs1064796690
openSNPrs1064796690
23andMers1064796690
23andMe allrs1064796690
SNPshotrs1064796690
SNPdbers1064796690
MSV3drs1064796690
GWAS Ctlgrs1064796690
Max Magnitude0
ClinVar
Risk rs1064796690(T;T)
Alt rs1064796690(T;T)
Reference Rs1064796690(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176707758C>T
CLNSRC
CLNACC RCV000482130.1,