Rs104894512

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894512(A;C)
Make rs104894512(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position21258785
GeneCRYM
is asnp
is mentioned by
dbSNPrs104894512
Exacrs104894512
PheGenIrs104894512
nextbiors104894512
hapmaprs104894512
1000 genomesrs104894512
hgdprs104894512
ensemblrs104894512
gopubmedrs104894512
geneviewrs104894512
scholarrs104894512
googlers104894512
pharmgkbrs104894512
gwascentralrs104894512
openSNPrs104894512
23andMers104894512
23andMe allrs104894512
SNP Nexus

SNPshotrs104894512
SNPdbers104894512
MSV3drs104894512
Merged fromRs28929490
OMIM123740
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894512(C;C)
Alt rs104894512(C;C)
Reference rs104894512(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene CRYM
CLNDBN Deafness, autosomal dominant nonsyndromic
Reversed 1
HGVS NC_000016.9:g.21270106T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018443.26,