Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518175(C;C)
Make rs1057518175(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177292163
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518175
dbSNP (old)rs1057518175
ClinGenrs1057518175
ebirs1057518175
HLIrs1057518175
Exacrs1057518175
Gnomadrs1057518175
Varsomers1057518175
LitVarrs1057518175
Maprs1057518175
PheGenIrs1057518175
Biobankrs1057518175
1000 genomesrs1057518175
hgdprs1057518175
ensemblrs1057518175
gopubmedrs1057518175
geneviewrs1057518175
scholarrs1057518175
googlers1057518175
pharmgkbrs1057518175
gwascentralrs1057518175
openSNPrs1057518175
23andMers1057518175
23andMe allrs1057518175
SNPshotrs1057518175
SNPdbers1057518175
MSV3drs1057518175
GWAS Ctlgrs1057518175
Max Magnitude0
ClinVar
Risk rs1057518175(C;C)
Alt rs1057518175(C;C)
Reference Rs1057518175(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176719164G>C
CLNSRC
CLNACC RCV000414523.1,