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rs1057517998

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517998(-;T)
Make rs1057517998(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177294333
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057517998
dbSNP (old)rs1057517998
ClinGenrs1057517998
ebirs1057517998
HLIrs1057517998
Exacrs1057517998
Gnomadrs1057517998
Varsomers1057517998
Maprs1057517998
PheGenIrs1057517998
Biobankrs1057517998
1000 genomesrs1057517998
hgdprs1057517998
ensemblrs1057517998
gopubmedrs1057517998
geneviewrs1057517998
scholarrs1057517998
googlers1057517998
pharmgkbrs1057517998
gwascentralrs1057517998
openSNPrs1057517998
23andMers1057517998
23andMe allrs1057517998
SNPshotrs1057517998
SNPdbers1057517998
MSV3drs1057517998
GWAS Ctlgrs1057517998
Max Magnitude0
ClinVar
Risk rs1057517998(T;T)
Alt rs1057517998(T;T)
Reference Rs1057517998(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176721334dupT
CLNSRC
CLNACC RCV000414751.1,