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rs1057518184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518184(C;GA)
Make rs1057518184(GA;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177257010
GeneNSD1
is asnp
is mentioned by
dbSNPrs1057518184
dbSNP (old)rs1057518184
ClinGenrs1057518184
ebirs1057518184
HLIrs1057518184
Exacrs1057518184
Gnomadrs1057518184
Varsomers1057518184
Maprs1057518184
PheGenIrs1057518184
Biobankrs1057518184
1000 genomesrs1057518184
hgdprs1057518184
ensemblrs1057518184
gopubmedrs1057518184
geneviewrs1057518184
scholarrs1057518184
googlers1057518184
pharmgkbrs1057518184
gwascentralrs1057518184
openSNPrs1057518184
23andMers1057518184
23andMe allrs1057518184
SNPshotrs1057518184
SNPdbers1057518184
MSV3drs1057518184
GWAS Ctlgrs1057518184
Max Magnitude0
ClinVar
Risk rs1057518184(GA;GA)
Alt rs1057518184(GA;GA)
Reference Rs1057518184(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176684011delCinsGA
CLNSRC
CLNACC RCV000414242.1,