rs377767440

Orientation

plus

Stabilized

plus

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

Make rs377767440(G;TTCT)

Make rs377767440(TTCT;TTCT)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114598

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767440
dbSNP (classic)	rs377767440
ClinGen	rs377767440
ebi	rs377767440
HLI	rs377767440
Exac	rs377767440
Gnomad	rs377767440
Varsome	rs377767440
LitVar	rs377767440
Map	rs377767440
PheGenI	rs377767440
Biobank	rs377767440
1000 genomes	rs377767440
hgdp	rs377767440
ensembl	rs377767440
geneview	rs377767440
scholar	rs377767440
google	rs377767440
pharmgkb	rs377767440
gwascentral	rs377767440
openSNP	rs377767440
23andMe	rs377767440
SNPshot	rs377767440
SNPdbe	rs377767440
MSV3d	rs377767440
GWAS Ctlg	rs377767440

Max Magnitude

0

ClinVar
Risk	rs377767440(TTCT;TTCT)
Alt	rs377767440(TTCT;TTCT)
Reference	Rs377767440(G;G)
Significance	Pathogenic
Disease	MEN2A and Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2A and Unclassified
Reversed	0
HGVS	NC_000010.10:g.43610046delGinsTTCT
CLNSRC	ClinVar
CLNACC	RCV000021840.1,