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rs1057518027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518027(A;A)
Make rs1057518027(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position72195460
GeneFOLR1
is asnp
is mentioned by
dbSNPrs1057518027
dbSNP (classic)rs1057518027
ClinGenrs1057518027
ebirs1057518027
HLIrs1057518027
Exacrs1057518027
Gnomadrs1057518027
Varsomers1057518027
LitVarrs1057518027
Maprs1057518027
PheGenIrs1057518027
Biobankrs1057518027
1000 genomesrs1057518027
hgdprs1057518027
ensemblrs1057518027
geneviewrs1057518027
scholarrs1057518027
googlers1057518027
pharmgkbrs1057518027
gwascentralrs1057518027
openSNPrs1057518027
23andMers1057518027
23andMe allrs1057518027
SNPshotrs1057518027
SNPdbers1057518027
MSV3drs1057518027
GWAS Ctlgrs1057518027
Max Magnitude0
ClinVar
Risk rs1057518027(A;A)
Alt rs1057518027(A;A)
Reference Rs1057518027(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOLR1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.71906504G>A
CLNSRC
CLNACC RCV000414186.1,