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rs1057518051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518051(A;C)
Make rs1057518051(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177292120
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518051
dbSNP (old)rs1057518051
ClinGenrs1057518051
ebirs1057518051
HLIrs1057518051
Exacrs1057518051
Gnomadrs1057518051
Varsomers1057518051
Maprs1057518051
PheGenIrs1057518051
Biobankrs1057518051
1000 genomesrs1057518051
hgdprs1057518051
ensemblrs1057518051
gopubmedrs1057518051
geneviewrs1057518051
scholarrs1057518051
googlers1057518051
pharmgkbrs1057518051
gwascentralrs1057518051
openSNPrs1057518051
23andMers1057518051
23andMe allrs1057518051
SNPshotrs1057518051
SNPdbers1057518051
MSV3drs1057518051
GWAS Ctlgrs1057518051
Max Magnitude0
ClinVar
Risk rs1057518051(C;C)
Alt rs1057518051(C;C)
Reference Rs1057518051(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176719121A>C
CLNSRC
CLNACC RCV000413194.1,