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rs786205648

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205648(-;-)
Make rs786205648(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177210221
GeneNSD1
is asnp
is mentioned by
dbSNPrs786205648
ebirs786205648
HLIrs786205648
Exacrs786205648
Varsomers786205648
Maprs786205648
PheGenIrs786205648
hapmaprs786205648
1000 genomesrs786205648
hgdprs786205648
ensemblrs786205648
gopubmedrs786205648
geneviewrs786205648
scholarrs786205648
googlers786205648
pharmgkbrs786205648
gwascentralrs786205648
openSNPrs786205648
23andMers786205648
23andMe allrs786205648
SNP Nexus

SNPshotrs786205648
SNPdbers786205648
MSV3drs786205648
GWAS Ctlgrs786205648
Max Magnitude0
ClinVar
Risk rs786205648(;)
Alt rs786205648(;)
Reference rs786205648(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176637222delA
CLNSRC
CLNACC RCV000171520.1,