rs104894509

Orientation

minus

Stabilized

minus

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

Make rs104894509(A;T)

Make rs104894509(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

21258781

Gene	CRYM, LOC105371124

is a	snp
is	mentioned by
dbSNP	rs104894509
dbSNP (classic)	rs104894509
ClinGen	rs104894509
ebi	rs104894509
HLI	rs104894509
Exac	rs104894509
Gnomad	rs104894509
Varsome	rs104894509
LitVar	rs104894509
Map	rs104894509
PheGenI	rs104894509
Biobank	rs104894509
1000 genomes	rs104894509
hgdp	rs104894509
ensembl	rs104894509
geneview	rs104894509
scholar	rs104894509
google	rs104894509
pharmgkb	rs104894509
gwascentral	rs104894509
openSNP	rs104894509
23andMe	rs104894509
SNPshot	rs104894509
SNPdbe	rs104894509
MSV3d	rs104894509
GWAS Ctlg	rs104894509

Max Magnitude

0

OMIM	123740
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894509(T;T)
Alt	rs104894509(T;T)
Reference	Rs104894509(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CRYM
CLNDBN	Deafness, autosomal dominant 40
Reversed	1
HGVS	NC_000016.9:g.21270102T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018442.24,