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rs727503935

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503935(A;A)
Make rs727503935(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28767949
GeneFOXG1
is asnp
is mentioned by
dbSNPrs727503935
ebirs727503935
HLIrs727503935
Exacrs727503935
Varsomers727503935
Maprs727503935
PheGenIrs727503935
hapmaprs727503935
1000 genomesrs727503935
hgdprs727503935
ensemblrs727503935
gopubmedrs727503935
geneviewrs727503935
scholarrs727503935
googlers727503935
pharmgkbrs727503935
gwascentralrs727503935
openSNPrs727503935
23andMers727503935
23andMe allrs727503935
SNP Nexus

SNPshotrs727503935
SNPdbers727503935
MSV3drs727503935
GWAS Ctlgrs727503935
Max Magnitude0
ClinVar
Risk rs727503935(A;A)
Alt rs727503935(A;A)
Reference rs727503935(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237155G>A
CLNSRC
CLNACC RCV000153265.3,