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rs1057518341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518341(C;C)
Make rs1057518341(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position97853346
GeneASNS
is asnp
is mentioned by
dbSNPrs1057518341
dbSNP (old)rs1057518341
ClinGenrs1057518341
ebirs1057518341
HLIrs1057518341
Exacrs1057518341
Gnomadrs1057518341
Varsomers1057518341
Maprs1057518341
PheGenIrs1057518341
Biobankrs1057518341
1000 genomesrs1057518341
hgdprs1057518341
ensemblrs1057518341
gopubmedrs1057518341
geneviewrs1057518341
scholarrs1057518341
googlers1057518341
pharmgkbrs1057518341
gwascentralrs1057518341
openSNPrs1057518341
23andMers1057518341
23andMe allrs1057518341
SNPshotrs1057518341
SNPdbers1057518341
MSV3drs1057518341
GWAS Ctlgrs1057518341
Max Magnitude0
ClinVar
Risk rs1057518341(C;C)
Alt rs1057518341(C;C)
Reference Rs1057518341(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASNS
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.97482658A>G
CLNSRC
CLNACC RCV000412830.1,