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rs587776626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776626(-;-)
Make rs587776626(-;G)
Make rs587776626(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position41746134
GenePHOX2B
is asnp
is mentioned by
dbSNPrs587776626
ebirs587776626
HLIrs587776626
Exacrs587776626
Varsomers587776626
Maprs587776626
PheGenIrs587776626
hapmaprs587776626
1000 genomesrs587776626
hgdprs587776626
ensemblrs587776626
gopubmedrs587776626
geneviewrs587776626
scholarrs587776626
googlers587776626
pharmgkbrs587776626
gwascentralrs587776626
openSNPrs587776626
23andMers587776626
23andMe allrs587776626
SNP Nexus

SNPshotrs587776626
SNPdbers587776626
MSV3drs587776626
GWAS Ctlgrs587776626
Max Magnitude0
ClinVar
Risk rs587776626(G;G)
Alt rs587776626(G;G)
Reference rs587776626(;)
Significance Pathogenic
Disease Congenital central hypoventilation
Variation info
Gene PHOX2B
CLNDBN Congenital central hypoventilation
Reversed 0
HGVS NC_000004.11:g.41748151dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000006380.3,