rs75686697

Orientation

plus

Stabilized

plus

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

Make rs75686697(A;A)

Make rs75686697(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43118420

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs75686697
dbSNP (classic)	rs75686697
ClinGen	rs75686697
ebi	rs75686697
HLI	rs75686697
Exac	rs75686697
Gnomad	rs75686697
Varsome	rs75686697
LitVar	rs75686697
Map	rs75686697
PheGenI	rs75686697
Biobank	rs75686697
1000 genomes	rs75686697
hgdp	rs75686697
ensembl	rs75686697
geneview	rs75686697
scholar	rs75686697
google	rs75686697
pharmgkb	rs75686697
gwascentral	rs75686697
openSNP	rs75686697
23andMe	rs75686697
SNPshot	rs75686697
SNPdbe	rs75686697
MSV3d	rs75686697
GWAS Ctlg	rs75686697

Max Magnitude

0

OMIM	164761
Desc
Variant	0053
Related	also

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 UniProtKB (protein)
CLNACC	RCV000014983.23, RCV000021847.1, RCV000206045.1,