rs79890926

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	5.1	Multiple Endocrine Neoplasia IIA

Make rs79890926(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113656

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs79890926
dbSNP (classic)	rs79890926
ClinGen	rs79890926
ebi	rs79890926
HLI	rs79890926
Exac	rs79890926
Gnomad	rs79890926
Varsome	rs79890926
LitVar	rs79890926
Map	rs79890926
PheGenI	rs79890926
Biobank	rs79890926
1000 genomes	rs79890926
hgdp	rs79890926
ensembl	rs79890926
geneview	rs79890926
scholar	rs79890926
google	rs79890926
pharmgkb	rs79890926
gwascentral	rs79890926
openSNP	rs79890926
23andMe	rs79890926
SNPshot	rs79890926
SNPdbe	rs79890926
MSV3d	rs79890926
GWAS Ctlg	rs79890926

Max Magnitude

5.1

OMIM	164761
Desc
Variant	0032
Related	also

ClinVar
Risk	rs79890926(G;G) rs79890926(T;T)
Alt	rs79890926(G;G) rs79890926(T;T)
Reference	Rs79890926(C;C)
Significance	Pathogenic
Disease	MULTIPLE ENDOCRINE NEOPLASIA MEN2A and Unclassified
Variation	info
Gene	RET
CLNDBN	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE MEN2A and Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609104C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014959.26, RCV000021789.1,