rs377767408

Orientation

plus

Stabilized

plus

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

Make rs377767408(CGTGC;CGTGC)

Make rs377767408(CGTGC;GCTGT)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114496

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767408
dbSNP (classic)	rs377767408
ClinGen	rs377767408
ebi	rs377767408
HLI	rs377767408
Exac	rs377767408
Gnomad	rs377767408
Varsome	rs377767408
LitVar	rs377767408
Map	rs377767408
PheGenI	rs377767408
Biobank	rs377767408
1000 genomes	rs377767408
hgdp	rs377767408
ensembl	rs377767408
geneview	rs377767408
scholar	rs377767408
google	rs377767408
pharmgkb	rs377767408
gwascentral	rs377767408
openSNP	rs377767408
23andMe	rs377767408
SNPshot	rs377767408
SNPdbe	rs377767408
MSV3d	rs377767408
GWAS Ctlg	rs377767408

Max Magnitude

0

ClinVar
Risk	rs377767408(CGTGC;CGTGC)
Alt	rs377767408(CGTGC;CGTGC)
Reference	Rs377767408(GCTGT;GCTGT)
Significance	Pathogenic
Disease	MEN2A and Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2A and Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609944_43609948delGCTGTinsCGTGC
CLNSRC	ClinVar
CLNACC	RCV000021819.1,