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rs76449634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs76449634(C;T)
Make rs76449634(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43102542
GeneRET
is asnp
is mentioned by
dbSNPrs76449634
ebirs76449634
HLIrs76449634
Exacrs76449634
Varsomers76449634
Maprs76449634
PheGenIrs76449634
hapmaprs76449634
1000 genomesrs76449634
hgdprs76449634
ensemblrs76449634
gopubmedrs76449634
geneviewrs76449634
scholarrs76449634
googlers76449634
pharmgkbrs76449634
gwascentralrs76449634
openSNPrs76449634
23andMers76449634
23andMe allrs76449634
SNP Nexus

SNPshotrs76449634
SNPdbers76449634
MSV3drs76449634
GWAS Ctlgrs76449634
Max Magnitude0
OMIM164761
Desc
Variant0021
Relatedalso
ClinVar
Risk rs76449634(T;T)
Alt rs76449634(T;T)
Reference rs76449634(C;C)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43597990C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014950.2,