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rs1057522318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522318(C;C)
Make rs1057522318(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position93585388
GeneNR2F1
is asnp
is mentioned by
dbSNPrs1057522318
dbSNP (old)rs1057522318
ClinGenrs1057522318
ebirs1057522318
HLIrs1057522318
Exacrs1057522318
Gnomadrs1057522318
Varsomers1057522318
LitVarrs1057522318
Maprs1057522318
PheGenIrs1057522318
Biobankrs1057522318
1000 genomesrs1057522318
hgdprs1057522318
ensemblrs1057522318
gopubmedrs1057522318
geneviewrs1057522318
scholarrs1057522318
googlers1057522318
pharmgkbrs1057522318
gwascentralrs1057522318
openSNPrs1057522318
23andMers1057522318
23andMe allrs1057522318
SNPshotrs1057522318
SNPdbers1057522318
MSV3drs1057522318
GWAS Ctlgrs1057522318
Max Magnitude0
ClinVar
Risk rs1057522318(C;C)
Alt rs1057522318(C;C)
Reference Rs1057522318(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NR2F1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.92921094G>C
CLNSRC
CLNACC RCV000439198.1,