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rs1057520710

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520710(C;C)
Make rs1057520710(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177267597
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057520710
dbSNP (old)rs1057520710
ClinGenrs1057520710
ebirs1057520710
HLIrs1057520710
Exacrs1057520710
Gnomadrs1057520710
Varsomers1057520710
Maprs1057520710
PheGenIrs1057520710
Biobankrs1057520710
1000 genomesrs1057520710
hgdprs1057520710
ensemblrs1057520710
gopubmedrs1057520710
geneviewrs1057520710
scholarrs1057520710
googlers1057520710
pharmgkbrs1057520710
gwascentralrs1057520710
openSNPrs1057520710
23andMers1057520710
23andMe allrs1057520710
SNPshotrs1057520710
SNPdbers1057520710
MSV3drs1057520710
GWAS Ctlgrs1057520710
Max Magnitude0
ClinVar
Risk rs1057520710(C;C)
Alt rs1057520710(C;C)
Reference Rs1057520710(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176694598G>C
CLNSRC
CLNACC RCV000427613.1,