rs387906358

Orientation

plus

Stabilized

plus

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

Make rs387906358(-;-)

Make rs387906358(-;TC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112088888

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs387906358
dbSNP (classic)	rs387906358
ClinGen	rs387906358
ebi	rs387906358
HLI	rs387906358
Exac	rs387906358
Gnomad	rs387906358
Varsome	rs387906358
LitVar	rs387906358
Map	rs387906358
PheGenI	rs387906358
Biobank	rs387906358
1000 genomes	rs387906358
hgdp	rs387906358
ensembl	rs387906358
geneview	rs387906358
scholar	rs387906358
google	rs387906358
pharmgkb	rs387906358
gwascentral	rs387906358
openSNP	rs387906358
23andMe	rs387906358
SNPshot	rs387906358
SNPdbe	rs387906358
MSV3d	rs387906358
GWAS Ctlg	rs387906358

Max Magnitude

0

ClinVar
Risk	rs387906358(-;-)
Alt	rs387906358(-;-)
Reference	Rs387906358(TC;TC)
Significance	Pathogenic
Disease	Paragangliomas 1 with sensorineural hearing loss not provided
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1 with sensorineural hearing loss not provided
Reversed	0
HGVS	NC_000011.9:g.111959612_111959613delTC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007313.2, RCV000481193.1,