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rs1057518286

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518286(A;G)
Make rs1057518286(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177291984
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518286
dbSNP (old)rs1057518286
ClinGenrs1057518286
ebirs1057518286
HLIrs1057518286
Exacrs1057518286
Gnomadrs1057518286
Varsomers1057518286
Maprs1057518286
PheGenIrs1057518286
Biobankrs1057518286
1000 genomesrs1057518286
hgdprs1057518286
ensemblrs1057518286
gopubmedrs1057518286
geneviewrs1057518286
scholarrs1057518286
googlers1057518286
pharmgkbrs1057518286
gwascentralrs1057518286
openSNPrs1057518286
23andMers1057518286
23andMe allrs1057518286
SNPshotrs1057518286
SNPdbers1057518286
MSV3drs1057518286
GWAS Ctlgrs1057518286
Max Magnitude0
ClinVar
Risk rs1057518286(G;G)
Alt rs1057518286(G;G)
Reference Rs1057518286(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176718985A>G
CLNSRC
CLNACC RCV000412899.1,