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rs1057518091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518091(A;A)
Make rs1057518091(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position37038743
GeneNIPBL
is asnp
is mentioned by
dbSNPrs1057518091
dbSNP (old)rs1057518091
ClinGenrs1057518091
ebirs1057518091
HLIrs1057518091
Exacrs1057518091
Gnomadrs1057518091
Varsomers1057518091
LitVarrs1057518091
Maprs1057518091
PheGenIrs1057518091
Biobankrs1057518091
1000 genomesrs1057518091
hgdprs1057518091
ensemblrs1057518091
gopubmedrs1057518091
geneviewrs1057518091
scholarrs1057518091
googlers1057518091
pharmgkbrs1057518091
gwascentralrs1057518091
openSNPrs1057518091
23andMers1057518091
23andMe allrs1057518091
SNPshotrs1057518091
SNPdbers1057518091
MSV3drs1057518091
GWAS Ctlgrs1057518091
Max Magnitude0
ClinVar
Risk rs1057518091(A;A)
Alt rs1057518091(A;A)
Reference Rs1057518091(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NIPBL
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.37038845G>A
CLNSRC
CLNACC RCV000414501.1,