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rs76736111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76736111(A;A)
Make rs76736111(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position43102596
GeneRET
is asnp
is mentioned by
dbSNPrs76736111
ebirs76736111
HLIrs76736111
Exacrs76736111
Varsomers76736111
Maprs76736111
PheGenIrs76736111
hapmaprs76736111
1000 genomesrs76736111
hgdprs76736111
ensemblrs76736111
gopubmedrs76736111
geneviewrs76736111
scholarrs76736111
googlers76736111
pharmgkbrs76736111
gwascentralrs76736111
openSNPrs76736111
23andMers76736111
23andMe allrs76736111
SNP Nexus

SNPshotrs76736111
SNPdbers76736111
MSV3drs76736111
GWAS Ctlgrs76736111
Max Magnitude0
OMIM164761
Desc
Variant0054
Relatedalso
ClinVar
Risk rs76736111(A;A)
Alt rs76736111(A;A)
Reference rs76736111(C;C)
Significance Pathogenic
Disease Renal adysplasia
Variation info
Gene RET
CLNDBN Renal adysplasia
Reversed 0
HGVS NC_000010.10:g.43598044C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014984.22,