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rs75686697

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs75686697(A;A)
Make rs75686697(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43118420
GeneRET
is asnp
is mentioned by
dbSNPrs75686697
ebirs75686697
HLIrs75686697
Exacrs75686697
Varsomers75686697
Maprs75686697
PheGenIrs75686697
hapmaprs75686697
1000 genomesrs75686697
hgdprs75686697
ensemblrs75686697
gopubmedrs75686697
geneviewrs75686697
scholarrs75686697
googlers75686697
pharmgkbrs75686697
gwascentralrs75686697
openSNPrs75686697
23andMers75686697
23andMe allrs75686697
SNP Nexus

SNPshotrs75686697
SNPdbers75686697
MSV3drs75686697
GWAS Ctlgrs75686697
Max Magnitude0
OMIM164761
Desc
Variant0053
Relatedalso
ClinVar
Risk rs75686697(A;A)
Alt rs75686697(A;A)
Reference rs75686697(G;G)
Significance Pathogenic
Disease Renal adysplasia MEN2 phenotype: Unknown Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Renal adysplasia MEN2 phenotype: Unknown Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43613868G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014983.22, RCV000021847.1, RCV000206045.1,