rs142318626

Orientation

plus

Stabilized

plus

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

Make rs142318626(C;T)

Make rs142318626(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

43119587

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs142318626
dbSNP (classic)	rs142318626
ClinGen	rs142318626
ebi	rs142318626
HLI	rs142318626
Exac	rs142318626
Gnomad	rs142318626
Varsome	rs142318626
LitVar	rs142318626
Map	rs142318626
PheGenI	rs142318626
Biobank	rs142318626
1000 genomes	rs142318626
hgdp	rs142318626
ensembl	rs142318626
geneview	rs142318626
scholar	rs142318626
google	rs142318626
pharmgkb	rs142318626
gwascentral	rs142318626
openSNP	rs142318626
23andMe	rs142318626
SNPshot	rs142318626
SNPdbe	rs142318626
MSV3d	rs142318626
GWAS Ctlg	rs142318626

Max Magnitude

0

ClinVar
Risk	rs142318626(T;T)
Alt	rs142318626(T;T)
Reference	Rs142318626(C;C)
Significance	Probable-Pathogenic
Disease	Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia not provided
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2 Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 2b not provided
Reversed	0
HGVS	NC_000010.10:g.43615035C>T
CLNSRC
CLNACC	RCV000123311.3, RCV000409506.1, RCV000411874.1, RCV000414497.1,