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rs11570255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11570255(A;A)
Make rs11570255(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position59300861
GeneEDN3
is asnp
is mentioned by
dbSNPrs11570255
ebirs11570255
HLIrs11570255
Exacrs11570255
Varsomers11570255
Maprs11570255
PheGenIrs11570255
hapmaprs11570255
1000 genomesrs11570255
hgdprs11570255
ensemblrs11570255
gopubmedrs11570255
geneviewrs11570255
scholarrs11570255
googlers11570255
pharmgkbrs11570255
gwascentralrs11570255
openSNPrs11570255
23andMers11570255
23andMe allrs11570255
SNP Nexus

SNPshotrs11570255
SNPdbers11570255
MSV3drs11570255
GWAS Ctlgrs11570255
GMAF0.00551
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM131242
DescHIRSCHSPRUNG DISEASE
Variant0004
Relatedalso


ClinVar
Risk rs11570255(A,T;A,T)
Alt rs11570255(A,T;A,T)
Reference rs11570255(G;G)
Significance Other
Disease Hirschsprung disease 4 not specified
Variation info
Gene EDN3
CLNDBN Hirschsprung disease 4 not specified
Reversed 0
HGVS NC_000020.10:g.57875916G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018126.2, RCV000222596.1,