Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520581(C;G)
Make rs1057520581(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177209796
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057520581
dbSNP (classic)rs1057520581
ClinGenrs1057520581
ebirs1057520581
HLIrs1057520581
Exacrs1057520581
Gnomadrs1057520581
Varsomers1057520581
LitVarrs1057520581
Maprs1057520581
PheGenIrs1057520581
Biobankrs1057520581
1000 genomesrs1057520581
hgdprs1057520581
ensemblrs1057520581
geneviewrs1057520581
scholarrs1057520581
googlers1057520581
pharmgkbrs1057520581
gwascentralrs1057520581
openSNPrs1057520581
23andMers1057520581
SNPshotrs1057520581
SNPdbers1057520581
MSV3drs1057520581
GWAS Ctlgrs1057520581
Max Magnitude0
ClinVar
Risk rs1057520581(G;G)
Alt rs1057520581(G;G)
Reference Rs1057520581(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176636797C>G
CLNSRC
CLNACC RCV000422342.1,