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rs786205576

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205576(A;A)
Make rs786205576(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177210457
GeneNSD1
is asnp
is mentioned by
dbSNPrs786205576
ebirs786205576
HLIrs786205576
Exacrs786205576
Varsomers786205576
Maprs786205576
PheGenIrs786205576
hapmaprs786205576
1000 genomesrs786205576
hgdprs786205576
ensemblrs786205576
gopubmedrs786205576
geneviewrs786205576
scholarrs786205576
googlers786205576
pharmgkbrs786205576
gwascentralrs786205576
openSNPrs786205576
23andMers786205576
23andMe allrs786205576
SNP Nexus

SNPshotrs786205576
SNPdbers786205576
MSV3drs786205576
GWAS Ctlgrs786205576
Max Magnitude0
ClinVar
Risk rs786205576(A;A)
Alt rs786205576(A;A)
Reference rs786205576(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176637458T>A
CLNSRC
CLNACC RCV000171389.1,