rs672601328

Merged into

rs377767434

Orientation

plus

Stabilized

plus

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

Make rs672601328(-;AGGAGTGTG)

Make rs672601328(AGGAGTGTG;AGGAGTGTG)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

43112170

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs672601328
dbSNP (classic)	rs672601328
ClinGen	rs672601328
ebi	rs672601328
HLI	rs672601328
Exac	rs672601328
Gnomad	rs672601328
Varsome	rs672601328
LitVar	rs672601328
Map	rs672601328
PheGenI	rs672601328
Biobank	rs672601328
1000 genomes	rs672601328
hgdp	rs672601328
ensembl	rs672601328
geneview	rs672601328
scholar	rs672601328
google	rs672601328
pharmgkb	rs672601328
gwascentral	rs672601328
openSNP	rs672601328
23andMe	rs672601328
SNPshot	rs672601328
SNPdbe	rs672601328
MSV3d	rs672601328
GWAS Ctlg	rs672601328

Status

Merged into rs377767434

Max Magnitude

0

ClinVar
Risk	rs672601328(GGAGTGTGA;GGAGTGTGA)
Alt	rs672601328(GGAGTGTGA;GGAGTGTGA)
Reference	Rs672601328(;)
Significance	Pathogenic
Disease	Familial medullary thyroid carcinoma
Variation	info
Gene	RET
CLNDBN	Familial medullary thyroid carcinoma
Reversed	0
HGVS	NC_000010.10:g.43607610_43607618dupAGGAGTGTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014968.26,