rs77711105

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs77711105(A;A)

Make rs77711105(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114542

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs77711105
dbSNP (classic)	rs77711105
ClinGen	rs77711105
ebi	rs77711105
HLI	rs77711105
Exac	rs77711105
Gnomad	rs77711105
Varsome	rs77711105
LitVar	rs77711105
Map	rs77711105
PheGenI	rs77711105
Biobank	rs77711105
1000 genomes	rs77711105
hgdp	rs77711105
ensembl	rs77711105
geneview	rs77711105
scholar	rs77711105
google	rs77711105
pharmgkb	rs77711105
gwascentral	rs77711105
openSNP	rs77711105
23andMe	rs77711105
SNPshot	rs77711105
SNPdbe	rs77711105
MSV3d	rs77711105
GWAS Ctlg	rs77711105

Max Magnitude

0

OMIM	164761
Desc
Variant	0047
Related	also

ClinVar
Risk	rs77711105(A;A)
Alt	rs77711105(A;A)
Reference	Rs77711105(G;G)
Significance	Other
Disease	Multiple endocrine neoplasia MEN2 phenotype: Unknown not provided Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia not specified
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a MEN2 phenotype: Unknown not provided Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 2 not specified
Reversed	0
HGVS	NC_000010.10:g.43609990G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014976.29, RCV000021834.1, RCV000034767.1, RCV000163319.3, RCV000198828.4, RCV000442648.1,