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rs1057519098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057519098(-;-)
Make rs1057519098(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position11753639
GeneGNAL
is asnp
is mentioned by
dbSNPrs1057519098
dbSNP (old)rs1057519098
ClinGenrs1057519098
ebirs1057519098
HLIrs1057519098
Exacrs1057519098
Gnomadrs1057519098
Varsomers1057519098
LitVarrs1057519098
Maprs1057519098
PheGenIrs1057519098
Biobankrs1057519098
1000 genomesrs1057519098
hgdprs1057519098
ensemblrs1057519098
gopubmedrs1057519098
geneviewrs1057519098
scholarrs1057519098
googlers1057519098
pharmgkbrs1057519098
gwascentralrs1057519098
openSNPrs1057519098
23andMers1057519098
23andMe allrs1057519098
SNPshotrs1057519098
SNPdbers1057519098
MSV3drs1057519098
GWAS Ctlgrs1057519098
Max Magnitude0
ClinVar
Risk rs1057519098(-;-)
Alt rs1057519098(-;-)
Reference Rs1057519098(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNAL
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.11753638_11753639delAG
CLNSRC
CLNACC RCV000416229.1,