Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894387

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104894387(G;T)
Make rs104894387(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position77901181
GeneEDNRB, SLFN14
is asnp
is mentioned by
dbSNPrs104894387
ebirs104894387
HLIrs104894387
Exacrs104894387
Varsomers104894387
Maprs104894387
PheGenIrs104894387
hapmaprs104894387
1000 genomesrs104894387
hgdprs104894387
ensemblrs104894387
gopubmedrs104894387
geneviewrs104894387
scholarrs104894387
googlers104894387
pharmgkbrs104894387
gwascentralrs104894387
openSNPrs104894387
23andMers104894387
23andMe allrs104894387
SNP Nexus

SNPshotrs104894387
SNPdbers104894387
MSV3drs104894387
GWAS Ctlgrs104894387
Max Magnitude0
OMIM131244
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894387(T;T)
Alt rs104894387(T;T)
Reference rs104894387(G;G)
Significance Other
Disease Hirschsprung disease 2 Waardenburg syndrome type 4A
Variation info
Gene EDNRB EDNRB-AS1
CLNDBN Hirschsprung disease 2 Waardenburg syndrome type 4A
Reversed 1
HGVS NC_000013.10:g.78475316C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018112.2, RCV000018113.27,