rs758906955
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs758906955(C;C) |
Make rs758906955(C;T) |
Make rs758906955(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 2 |
Position | 165097377 |
Gene | SCN3A |
is a | snp |
is | mentioned by |
dbSNP | rs758906955 |
dbSNP (classic) | rs758906955 |
ClinGen | rs758906955 |
ebi | rs758906955 |
HLI | rs758906955 |
Exac | rs758906955 |
Gnomad | rs758906955 |
Varsome | rs758906955 |
LitVar | rs758906955 |
Map | rs758906955 |
PheGenI | rs758906955 |
Biobank | rs758906955 |
1000 genomes | rs758906955 |
hgdp | rs758906955 |
ensembl | rs758906955 |
geneview | rs758906955 |
scholar | rs758906955 |
rs758906955 | |
pharmgkb | rs758906955 |
gwascentral | rs758906955 |
openSNP | rs758906955 |
23andMe | rs758906955 |
SNPshot | rs758906955 |
SNPdbe | rs758906955 |
MSV3d | rs758906955 |
GWAS Ctlg | rs758906955 |
Max Magnitude | 0 |
aka NM_006922.3(SCN3A):c.4114A>G or (p.Met1372Val)
OMIM pathogenic variant