rs193922700

Orientation

plus

Stabilized

plus

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

Make rs193922700(C;T)

Make rs193922700(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114680

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs193922700
dbSNP (classic)	rs193922700
ClinGen	rs193922700
ebi	rs193922700
HLI	rs193922700
Exac	rs193922700
Gnomad	rs193922700
Varsome	rs193922700
LitVar	rs193922700
Map	rs193922700
PheGenI	rs193922700
Biobank	rs193922700
1000 genomes	rs193922700
hgdp	rs193922700
ensembl	rs193922700
geneview	rs193922700
scholar	rs193922700
google	rs193922700
pharmgkb	rs193922700
gwascentral	rs193922700
openSNP	rs193922700
23andMe	rs193922700
SNPshot	rs193922700
SNPdbe	rs193922700
MSV3d	rs193922700
GWAS Ctlg	rs193922700

Max Magnitude

0

ClinVar
Risk	rs193922700(T;T)
Alt	rs193922700(T;T)
Reference	Rs193922700(C;C)
Significance	Probable-Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a
Reversed	0
HGVS	NC_000010.10:g.43610128C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030406.1,