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

rs76087194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs76087194(A;A)
Make rs76087194(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43120163
GeneRET
is asnp
is mentioned by
dbSNPrs76087194
ebirs76087194
HLIrs76087194
Exacrs76087194
Varsomers76087194
Maprs76087194
PheGenIrs76087194
hapmaprs76087194
1000 genomesrs76087194
hgdprs76087194
ensemblrs76087194
gopubmedrs76087194
geneviewrs76087194
scholarrs76087194
googlers76087194
pharmgkbrs76087194
gwascentralrs76087194
openSNPrs76087194
23andMers76087194
23andMe allrs76087194
SNP Nexus

SNPshotrs76087194
SNPdbers76087194
MSV3drs76087194
GWAS Ctlgrs76087194
Max Magnitude0
OMIM164761
Desc
Variant0016
Relatedalso
ClinVar
Risk rs76087194(A;A)
Alt rs76087194(A;A)
Reference rs76087194(G;G)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43615611G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014946.2,