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rs752611838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752611838(A;A)
Make rs752611838(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63944804
GeneSCN4A
is asnp
is mentioned by
dbSNPrs752611838
dbSNP (classic)rs752611838
ClinGenrs752611838
ebirs752611838
HLIrs752611838
Exacrs752611838
Gnomadrs752611838
Varsomers752611838
LitVarrs752611838
Maprs752611838
PheGenIrs752611838
Biobankrs752611838
1000 genomesrs752611838
hgdprs752611838
ensemblrs752611838
geneviewrs752611838
scholarrs752611838
googlers752611838
pharmgkbrs752611838
gwascentralrs752611838
openSNPrs752611838
23andMers752611838
23andMe allrs752611838
SNPshotrs752611838
SNPdbers752611838
MSV3drs752611838
GWAS Ctlgrs752611838
Max Magnitude0
ClinVar
Risk rs752611838(A;A)
Alt rs752611838(A;A)
Reference Rs752611838(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.62022164C>A
CLNSRC
CLNACC RCV000493171.1,