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rs1057520620

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520620(A;A)
Make rs1057520620(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177283786
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057520620
dbSNP (old)rs1057520620
ClinGenrs1057520620
ebirs1057520620
HLIrs1057520620
Exacrs1057520620
Gnomadrs1057520620
Varsomers1057520620
Maprs1057520620
PheGenIrs1057520620
Biobankrs1057520620
1000 genomesrs1057520620
hgdprs1057520620
ensemblrs1057520620
gopubmedrs1057520620
geneviewrs1057520620
scholarrs1057520620
googlers1057520620
pharmgkbrs1057520620
gwascentralrs1057520620
openSNPrs1057520620
23andMers1057520620
23andMe allrs1057520620
SNPshotrs1057520620
SNPdbers1057520620
MSV3drs1057520620
GWAS Ctlgrs1057520620
Max Magnitude0
ClinVar
Risk rs1057520620(A;A)
Alt rs1057520620(A;A)
Reference Rs1057520620(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176710787G>A
CLNSRC
CLNACC RCV000421475.1,