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rs77596424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs77596424(C;T)
Make rs77596424(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43100576
GeneRET
is asnp
is mentioned by
dbSNPrs77596424
ebirs77596424
HLIrs77596424
Exacrs77596424
Varsomers77596424
Maprs77596424
PheGenIrs77596424
hapmaprs77596424
1000 genomesrs77596424
hgdprs77596424
ensemblrs77596424
gopubmedrs77596424
geneviewrs77596424
scholarrs77596424
googlers77596424
pharmgkbrs77596424
gwascentralrs77596424
openSNPrs77596424
23andMers77596424
23andMe allrs77596424
SNP Nexus

SNPshotrs77596424
SNPdbers77596424
MSV3drs77596424
GWAS Ctlgrs77596424
Max Magnitude0
OMIM164761
Desc
Variant0019
Relatedalso
ClinVar
Risk rs77596424(T;T)
Alt rs77596424(T;T)
Reference rs77596424(C;C)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43596024C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014949.2,