rs745434198

Orientation

plus

Stabilized

plus

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

Make rs745434198(A;A)

Make rs745434198(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

33165983

Gene

COL11A2

is a	snp
is	mentioned by
dbSNP	rs745434198
dbSNP (classic)	rs745434198
ClinGen	rs745434198
ebi	rs745434198
HLI	rs745434198
Exac	rs745434198
Gnomad	rs745434198
Varsome	rs745434198
LitVar	rs745434198
Map	rs745434198
PheGenI	rs745434198
Biobank	rs745434198
1000 genomes	rs745434198
hgdp	rs745434198
ensembl	rs745434198
geneview	rs745434198
scholar	rs745434198
google	rs745434198
pharmgkb	rs745434198
gwascentral	rs745434198
openSNP	rs745434198
23andMe	rs745434198
SNPshot	rs745434198
SNPdbe	rs745434198
MSV3d	rs745434198
GWAS Ctlg	rs745434198

Max Magnitude

0

ClinVar
Risk	rs745434198(A;A)
Alt	rs745434198(A;A)
Reference	Rs745434198(C;C)
Significance	Probable-Pathogenic
Disease	Sensorineural hearing impairment
Variation	info
Gene	COL11A2
CLNDBN	Sensorineural hearing impairment
Reversed	0
HGVS	NC_000006.11:g.33133760C>A
CLNSRC
CLNACC	RCV000415302.1,