rs377767397

Orientation

plus

Stabilized

plus

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

Make rs377767397(A;A)

Make rs377767397(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113628

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767397
dbSNP (classic)	rs377767397
ClinGen	rs377767397
ebi	rs377767397
HLI	rs377767397
Exac	rs377767397
Gnomad	rs377767397
Varsome	rs377767397
LitVar	rs377767397
Map	rs377767397
PheGenI	rs377767397
Biobank	rs377767397
1000 genomes	rs377767397
hgdp	rs377767397
ensembl	rs377767397
geneview	rs377767397
scholar	rs377767397
google	rs377767397
pharmgkb	rs377767397
gwascentral	rs377767397
openSNP	rs377767397
23andMe	rs377767397
SNPshot	rs377767397
SNPdbe	rs377767397
MSV3d	rs377767397
GWAS Ctlg	rs377767397

Max Magnitude

0

ClinVar
Risk	rs377767397(A;A) rs377767397(C;C) rs377767397(T;T)
Alt	rs377767397(A;A) rs377767397(C;C) rs377767397(T;T)
Reference	Rs377767397(G;G)
Significance	Pathogenic
Disease	MEN2A and FMTC not provided MEN2 phenotype: Unknown
Variation	info
Gene	RET
CLNDBN	MEN2A and FMTC not provided MEN2 phenotype: Unknown
Reversed	0
HGVS	NC_000010.10:g.43609076G>A; NC_000010.10:g.43609076G>C; NC_000010.10:g.43609076G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000021784.1, RCV000412987.1, RCV000021786.1, RCV000021787.1,