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rs1057524829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524829(A;G)
Make rs1057524829(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position72192174
GeneFOLR1
is asnp
is mentioned by
dbSNPrs1057524829
dbSNP (classic)rs1057524829
ClinGenrs1057524829
ebirs1057524829
HLIrs1057524829
Exacrs1057524829
Gnomadrs1057524829
Varsomers1057524829
LitVarrs1057524829
Maprs1057524829
PheGenIrs1057524829
Biobankrs1057524829
1000 genomesrs1057524829
hgdprs1057524829
ensemblrs1057524829
geneviewrs1057524829
scholarrs1057524829
googlers1057524829
pharmgkbrs1057524829
gwascentralrs1057524829
openSNPrs1057524829
23andMers1057524829
23andMe allrs1057524829
SNPshotrs1057524829
SNPdbers1057524829
MSV3drs1057524829
GWAS Ctlgrs1057524829
Max Magnitude0
ClinVar
Risk rs1057524829(G;G)
Alt rs1057524829(G;G)
Reference Rs1057524829(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOLR1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.71903218A>G
CLNSRC
CLNACC RCV000427429.1,