rs77503355

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	5.1	Multiple Endocrine Neoplasia IIA
(C;G)	5.1	Multiple Endocrine Neoplasia IIA
(G;G)	0	common in clinvar
(G;T)	5.1	Multiple Endocrine Neoplasia IIA

Make rs77503355(A;A)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113655

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs77503355
dbSNP (classic)	rs77503355
ClinGen	rs77503355
ebi	rs77503355
HLI	rs77503355
Exac	rs77503355
Gnomad	rs77503355
Varsome	rs77503355
LitVar	rs77503355
Map	rs77503355
PheGenI	rs77503355
Biobank	rs77503355
1000 genomes	rs77503355
hgdp	rs77503355
ensembl	rs77503355
geneview	rs77503355
scholar	rs77503355
google	rs77503355
pharmgkb	rs77503355
gwascentral	rs77503355
openSNP	rs77503355
23andMe	rs77503355
SNPshot	rs77503355
SNPdbe	rs77503355
MSV3d	rs77503355
GWAS Ctlg	rs77503355

Max Magnitude

5.1

OMIM	164761
Desc
Variant	0024
Related	also

OMIM	164761
Desc
Variant	0041
Related	also

ClinVar
Risk	rs77503355(A;A) rs77503355(C;C) rs77503355(T;T)
Alt	rs77503355(A;A) rs77503355(C;C) rs77503355(T;T)
Reference	Rs77503355(G;G)
Significance	Other
Disease	Multiple endocrine neoplasia MEN2A and FMTC not provided Medullary thyroid carcinoma Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia Familial medullary thyroid carcinoma Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a MEN2A and FMTC not provided Medullary thyroid carcinoma Multiple endocrine neoplasia, type 1 Multiple endocrine neoplasia, type 2b Multiple endocrine neoplasia, type 4 Familial medullary thyroid carcinoma Multiple endocrine neoplasia, type 2
Reversed	0
HGVS	NC_000010.10:g.43609103G>A; NC_000010.10:g.43609103G>C; NC_000010.10:g.43609103G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein) HGMD
CLNACC	RCV000014936.25, RCV000021801.1, RCV000413879.1, RCV000420281.1, RCV000428368.1, RCV000431330.1, RCV000441133.1, RCV000014970.23, RCV000021802.1, RCV000489707.1, RCV000014953.26, RCV000021803.1, RCV000153834.5, RCV000233944.2, RCV000411165.1, RCV000485714.1,