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rs1057518133

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518133(G;T)
Make rs1057518133(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177260151
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518133
dbSNP (old)rs1057518133
ClinGenrs1057518133
ebirs1057518133
HLIrs1057518133
Exacrs1057518133
Gnomadrs1057518133
Varsomers1057518133
Maprs1057518133
PheGenIrs1057518133
Biobankrs1057518133
1000 genomesrs1057518133
hgdprs1057518133
ensemblrs1057518133
gopubmedrs1057518133
geneviewrs1057518133
scholarrs1057518133
googlers1057518133
pharmgkbrs1057518133
gwascentralrs1057518133
openSNPrs1057518133
23andMers1057518133
23andMe allrs1057518133
SNPshotrs1057518133
SNPdbers1057518133
MSV3drs1057518133
GWAS Ctlgrs1057518133
Max Magnitude0
ClinVar
Risk rs1057518133(T;T)
Alt rs1057518133(T;T)
Reference Rs1057518133(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176687152G>T
CLNSRC
CLNACC RCV000414147.1,