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rs79014735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs79014735(G;T)
Make rs79014735(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43102410
GeneRET
is asnp
is mentioned by
dbSNPrs79014735
ebirs79014735
HLIrs79014735
Exacrs79014735
Varsomers79014735
Maprs79014735
PheGenIrs79014735
hapmaprs79014735
1000 genomesrs79014735
hgdprs79014735
ensemblrs79014735
gopubmedrs79014735
geneviewrs79014735
scholarrs79014735
googlers79014735
pharmgkbrs79014735
gwascentralrs79014735
openSNPrs79014735
23andMers79014735
23andMe allrs79014735
SNP Nexus

SNPshotrs79014735
SNPdbers79014735
MSV3drs79014735
GWAS Ctlgrs79014735
Max Magnitude0
OMIM164761
Desc
Variant0020
Relatedalso
ClinVar
Risk rs79014735(A,T;A,T)
Alt rs79014735(A,T;A,T)
Reference rs79014735(G;G)
Significance Other
Disease Multiple endocrine neoplasia Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2 Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43597858G>A; NC_000010.10:g.43597858G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000197380.1, RCV000014931.2,