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rs773770609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773770609(A;A)
Make rs773770609(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position6695784
GeneSLC13A5
is asnp
is mentioned by
dbSNPrs773770609
dbSNP (classic)rs773770609
ClinGenrs773770609
ebirs773770609
HLIrs773770609
Exacrs773770609
Gnomadrs773770609
Varsomers773770609
LitVarrs773770609
Maprs773770609
PheGenIrs773770609
Biobankrs773770609
1000 genomesrs773770609
hgdprs773770609
ensemblrs773770609
geneviewrs773770609
scholarrs773770609
googlers773770609
pharmgkbrs773770609
gwascentralrs773770609
openSNPrs773770609
23andMers773770609
SNPshotrs773770609
SNPdbers773770609
MSV3drs773770609
GWAS Ctlgrs773770609
Max Magnitude0
ClinVar
Risk rs773770609(A;A)
Alt rs773770609(A;A)
Reference Rs773770609(G;G)
Significance Pathogenic
Disease not provided Epileptic encephalopathy
Variation info
Gene SLC13A5
CLNDBN not provided Epileptic encephalopathy, early infantile, 25
Reversed 0
HGVS NC_000017.10:g.6599103G>A
CLNSRC
CLNACC RCV000368574.1, RCV000416469.1,