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rs757611751

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757611751(A;C)
Make rs757611751(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position91055962
GeneKERA
is asnp
is mentioned by
dbSNPrs757611751
ebirs757611751
HLIrs757611751
Exacrs757611751
Varsomers757611751
Maprs757611751
PheGenIrs757611751
hapmaprs757611751
1000 genomesrs757611751
hgdprs757611751
ensemblrs757611751
gopubmedrs757611751
geneviewrs757611751
scholarrs757611751
googlers757611751
pharmgkbrs757611751
gwascentralrs757611751
openSNPrs757611751
23andMers757611751
23andMe allrs757611751
SNP Nexus

SNPshotrs757611751
SNPdbers757611751
MSV3drs757611751
GWAS Ctlgrs757611751
Max Magnitude0
ClinVar
Risk rs757611751(C;C)
Alt rs757611751(C;C)
Reference rs757611751(A;A)
Significance Pathogenic
Disease Cornea plana 2
Variation info
Gene KERA
CLNDBN Cornea plana 2
Reversed 0
HGVS NC_000012.11:g.91449739A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210915.1,