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rs1057518816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518816(A;A)
Make rs1057518816(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position72195389
GeneFOLR1
is asnp
is mentioned by
dbSNPrs1057518816
dbSNP (old)rs1057518816
ClinGenrs1057518816
ebirs1057518816
HLIrs1057518816
Exacrs1057518816
Gnomadrs1057518816
Varsomers1057518816
Maprs1057518816
PheGenIrs1057518816
Biobankrs1057518816
1000 genomesrs1057518816
hgdprs1057518816
ensemblrs1057518816
gopubmedrs1057518816
geneviewrs1057518816
scholarrs1057518816
googlers1057518816
pharmgkbrs1057518816
gwascentralrs1057518816
openSNPrs1057518816
23andMers1057518816
23andMe allrs1057518816
SNPshotrs1057518816
SNPdbers1057518816
MSV3drs1057518816
GWAS Ctlgrs1057518816
Max Magnitude0
ClinVar
Risk rs1057518816(A;A)
Alt rs1057518816(A;A)
Reference Rs1057518816(G;G)
Significance Probable-Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene FOLR1
CLNDBN Epileptic encephalopathy
Reversed 0
HGVS NC_000011.9:g.71906433G>A
CLNSRC
CLNACC RCV000415252.1,