Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520671(A;A)
Make rs1057520671(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177251854
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057520671
dbSNP (old)rs1057520671
ClinGenrs1057520671
ebirs1057520671
HLIrs1057520671
Exacrs1057520671
Gnomadrs1057520671
Varsomers1057520671
Maprs1057520671
PheGenIrs1057520671
Biobankrs1057520671
1000 genomesrs1057520671
hgdprs1057520671
ensemblrs1057520671
gopubmedrs1057520671
geneviewrs1057520671
scholarrs1057520671
googlers1057520671
pharmgkbrs1057520671
gwascentralrs1057520671
openSNPrs1057520671
23andMers1057520671
23andMe allrs1057520671
SNPshotrs1057520671
SNPdbers1057520671
MSV3drs1057520671
GWAS Ctlgrs1057520671
Max Magnitude0
ClinVar
Risk rs1057520671(A;A)
Alt rs1057520671(A;A)
Reference Rs1057520671(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176678855G>A
CLNSRC
CLNACC RCV000435432.1,