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rs864622785

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622785(G;G)
Make rs864622785(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position63964600
GeneLOC105371858, SCN4A
is asnp
is mentioned by
dbSNPrs864622785
ebirs864622785
HLIrs864622785
Exacrs864622785
Varsomers864622785
Maprs864622785
PheGenIrs864622785
hapmaprs864622785
1000 genomesrs864622785
hgdprs864622785
ensemblrs864622785
gopubmedrs864622785
geneviewrs864622785
scholarrs864622785
googlers864622785
pharmgkbrs864622785
gwascentralrs864622785
openSNPrs864622785
23andMers864622785
23andMe allrs864622785
SNP Nexus

SNPshotrs864622785
SNPdbers864622785
MSV3drs864622785
GWAS Ctlgrs864622785
Max Magnitude0
ClinVar
Risk rs864622785(G;G)
Alt rs864622785(G;G)
Reference rs864622785(T;T)
Significance Pathogenic
Disease Hyperkalemic Periodic Paralysis Type 1
Variation info
Gene SCN4A
CLNDBN Hyperkalemic Periodic Paralysis Type 1
Reversed 1
HGVS NC_000017.10:g.62041960A>C
CLNSRC
CLNACC RCV000207008.1,