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rs1057521142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521142(A;G)
Make rs1057521142(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177273771
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057521142
dbSNP (classic)rs1057521142
ClinGenrs1057521142
ebirs1057521142
HLIrs1057521142
Exacrs1057521142
Gnomadrs1057521142
Varsomers1057521142
LitVarrs1057521142
Maprs1057521142
PheGenIrs1057521142
Biobankrs1057521142
1000 genomesrs1057521142
hgdprs1057521142
ensemblrs1057521142
geneviewrs1057521142
scholarrs1057521142
googlers1057521142
pharmgkbrs1057521142
gwascentralrs1057521142
openSNPrs1057521142
23andMers1057521142
23andMe allrs1057521142
SNPshotrs1057521142
SNPdbers1057521142
MSV3drs1057521142
GWAS Ctlgrs1057521142
Max Magnitude0
ClinVar
Risk rs1057521142(G;G)
Alt rs1057521142(G;G)
Reference Rs1057521142(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176700772A>G
CLNSRC
CLNACC RCV000425262.1,