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rs781379291

From SNPedia

Orientationplus
Stabilizedplus
Make rs781379291(A;A)
Make rs781379291(A;G)
Make rs781379291(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome11
Position35292512
GeneSLC1A2
is asnp
is mentioned by
dbSNPrs781379291
dbSNP (classic)rs781379291
ClinGenrs781379291
ebirs781379291
HLIrs781379291
Exacrs781379291
Gnomadrs781379291
Varsomers781379291
LitVarrs781379291
Maprs781379291
PheGenIrs781379291
Biobankrs781379291
1000 genomesrs781379291
hgdprs781379291
ensemblrs781379291
geneviewrs781379291
scholarrs781379291
googlers781379291
pharmgkbrs781379291
gwascentralrs781379291
openSNPrs781379291
23andMers781379291
23andMe allrs781379291
SNPshotrs781379291
SNPdbers781379291
MSV3drs781379291
GWAS Ctlgrs781379291
Max Magnitude0

aka NM_004171.3(SLC1A2):c.866C>G or (p.Pro289Arg)

OMIM pathogenic variant