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rs1057518052

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518052(A;T)
Make rs1057518052(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177283835
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518052
dbSNP (old)rs1057518052
ClinGenrs1057518052
ebirs1057518052
HLIrs1057518052
Exacrs1057518052
Gnomadrs1057518052
Varsomers1057518052
Maprs1057518052
PheGenIrs1057518052
Biobankrs1057518052
1000 genomesrs1057518052
hgdprs1057518052
ensemblrs1057518052
gopubmedrs1057518052
geneviewrs1057518052
scholarrs1057518052
googlers1057518052
pharmgkbrs1057518052
gwascentralrs1057518052
openSNPrs1057518052
23andMers1057518052
23andMe allrs1057518052
SNPshotrs1057518052
SNPdbers1057518052
MSV3drs1057518052
GWAS Ctlgrs1057518052
Max Magnitude0
ClinVar
Risk rs1057518052(T;T)
Alt rs1057518052(T;T)
Reference Rs1057518052(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176710836A>T
CLNSRC
CLNACC RCV000414652.1,