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rs1057518196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs1057518196(CG;GTC)
Make rs1057518196(GTC;GTC)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28768439
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057518196
dbSNP (old)rs1057518196
ClinGenrs1057518196
ebirs1057518196
HLIrs1057518196
Exacrs1057518196
Gnomadrs1057518196
Varsomers1057518196
LitVarrs1057518196
Maprs1057518196
PheGenIrs1057518196
Biobankrs1057518196
1000 genomesrs1057518196
hgdprs1057518196
ensemblrs1057518196
gopubmedrs1057518196
geneviewrs1057518196
scholarrs1057518196
googlers1057518196
pharmgkbrs1057518196
gwascentralrs1057518196
openSNPrs1057518196
23andMers1057518196
23andMe allrs1057518196
SNPshotrs1057518196
SNPdbers1057518196
MSV3drs1057518196
GWAS Ctlgrs1057518196
Max Magnitude0
ClinVar
Risk rs1057518196(GTC;GTC)
Alt rs1057518196(GTC;GTC)
Reference Rs1057518196(CG;CG)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237645_29237646delCGinsGTC
CLNSRC
CLNACC RCV000414221.1,