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rs1057521243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521243(C;C)
Make rs1057521243(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position2665371
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs1057521243
dbSNP (old)rs1057521243
ClinGenrs1057521243
ebirs1057521243
HLIrs1057521243
Exacrs1057521243
Gnomadrs1057521243
Varsomers1057521243
Maprs1057521243
PheGenIrs1057521243
Biobankrs1057521243
1000 genomesrs1057521243
hgdprs1057521243
ensemblrs1057521243
gopubmedrs1057521243
geneviewrs1057521243
scholarrs1057521243
googlers1057521243
pharmgkbrs1057521243
gwascentralrs1057521243
openSNPrs1057521243
23andMers1057521243
23andMe allrs1057521243
SNPshotrs1057521243
SNPdbers1057521243
MSV3drs1057521243
GWAS Ctlgrs1057521243
Max Magnitude0
ClinVar
Risk rs1057521243(C;C)
Alt rs1057521243(C;C)
Reference Rs1057521243(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAFAH1B1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.2568665G>C
CLNSRC
CLNACC RCV000441930.1,