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rs758906955

From SNPedia

Orientationplus
Stabilizedplus
Make rs758906955(C;C)
Make rs758906955(C;T)
Make rs758906955(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome2
Position165097377
GeneSCN3A
is asnp
is mentioned by
dbSNPrs758906955
dbSNP (classic)rs758906955
ClinGenrs758906955
ebirs758906955
HLIrs758906955
Exacrs758906955
Gnomadrs758906955
Varsomers758906955
LitVarrs758906955
Maprs758906955
PheGenIrs758906955
Biobankrs758906955
1000 genomesrs758906955
hgdprs758906955
ensemblrs758906955
geneviewrs758906955
scholarrs758906955
googlers758906955
pharmgkbrs758906955
gwascentralrs758906955
openSNPrs758906955
23andMers758906955
23andMe allrs758906955
SNPshotrs758906955
SNPdbers758906955
MSV3drs758906955
GWAS Ctlgrs758906955
Max Magnitude0

aka NM_006922.3(SCN3A):c.4114A>G or (p.Met1372Val)

OMIM pathogenic variant