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

rs78098482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs78098482(A;A)
Make rs78098482(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position43109146
GeneRET
is asnp
is mentioned by
dbSNPrs78098482
ebirs78098482
HLIrs78098482
Exacrs78098482
Varsomers78098482
Maprs78098482
PheGenIrs78098482
hapmaprs78098482
1000 genomesrs78098482
hgdprs78098482
ensemblrs78098482
gopubmedrs78098482
geneviewrs78098482
scholarrs78098482
googlers78098482
pharmgkbrs78098482
gwascentralrs78098482
openSNPrs78098482
23andMers78098482
23andMe allrs78098482
SNP Nexus

SNPshotrs78098482
SNPdbers78098482
MSV3drs78098482
GWAS Ctlgrs78098482
Max Magnitude0
OMIM164761
Desc
Variant0023
Relatedalso
ClinVar
Risk rs78098482(A;A)
Alt rs78098482(A;A)
Reference rs78098482(C;C)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43604594C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014952.2,