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rs775803239

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775803239(A;A)
Make rs775803239(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position73323289
GeneHCN4
is asnp
is mentioned by
dbSNPrs775803239
ebirs775803239
HLIrs775803239
Exacrs775803239
Varsomers775803239
Maprs775803239
PheGenIrs775803239
hapmaprs775803239
1000 genomesrs775803239
hgdprs775803239
ensemblrs775803239
gopubmedrs775803239
geneviewrs775803239
scholarrs775803239
googlers775803239
pharmgkbrs775803239
gwascentralrs775803239
openSNPrs775803239
23andMers775803239
23andMe allrs775803239
SNP Nexus

SNPshotrs775803239
SNPdbers775803239
MSV3drs775803239
GWAS Ctlgrs775803239
Max Magnitude0
ClinVar
Risk rs775803239(A;A) rs775803239(T;T)
Alt rs775803239(A;A) rs775803239(T;T)
Reference Rs775803239(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene HCN4
CLNDBN not provided not specified
Reversed 0
HGVS NC_000015.9:g.73615630G>A
CLNSRC
CLNACC RCV000170943.2, RCV000223698.1,