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rs786205835

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205835(A;A)
Make rs786205835(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position35039116
GeneHPN, SCN1B
is asnp
is mentioned by
dbSNPrs786205835
ebirs786205835
HLIrs786205835
Exacrs786205835
Varsomers786205835
Maprs786205835
PheGenIrs786205835
hapmaprs786205835
1000 genomesrs786205835
hgdprs786205835
ensemblrs786205835
gopubmedrs786205835
geneviewrs786205835
scholarrs786205835
googlers786205835
pharmgkbrs786205835
gwascentralrs786205835
openSNPrs786205835
23andMers786205835
23andMe allrs786205835
SNP Nexus

SNPshotrs786205835
SNPdbers786205835
MSV3drs786205835
GWAS Ctlgrs786205835
Max Magnitude0
ClinVar
Risk rs786205835(A;A)
Alt rs786205835(A;A)
Reference rs786205835(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1B HPN
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.35530020G>A
CLNSRC
CLNACC RCV000171051.2,