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rs76764689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs76764689(C;T)
Make rs76764689(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43100480
GeneRET
is asnp
is mentioned by
dbSNPrs76764689
ebirs76764689
HLIrs76764689
Exacrs76764689
Varsomers76764689
Maprs76764689
PheGenIrs76764689
hapmaprs76764689
1000 genomesrs76764689
hgdprs76764689
ensemblrs76764689
gopubmedrs76764689
geneviewrs76764689
scholarrs76764689
googlers76764689
pharmgkbrs76764689
gwascentralrs76764689
openSNPrs76764689
23andMers76764689
23andMe allrs76764689
SNP Nexus

SNPshotrs76764689
SNPdbers76764689
MSV3drs76764689
GWAS Ctlgrs76764689
Max Magnitude0
OMIM164761
Desc
Variant0018
Relatedalso
ClinVar
Risk rs76764689(T;T)
Alt rs76764689(T;T)
Reference rs76764689(C;C)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43595928C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014948.2,