Have questions? Visit https://www.reddit.com/r/SNPedia

rs149364215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149364215(A;A)
Make rs149364215(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position13947661
GeneERCC4
is asnp
is mentioned by
dbSNPrs149364215
ebirs149364215
HLIrs149364215
Exacrs149364215
Varsomers149364215
Maprs149364215
PheGenIrs149364215
hapmaprs149364215
1000 genomesrs149364215
hgdprs149364215
ensemblrs149364215
gopubmedrs149364215
geneviewrs149364215
scholarrs149364215
googlers149364215
pharmgkbrs149364215
gwascentralrs149364215
openSNPrs149364215
23andMers149364215
23andMe allrs149364215
SNP Nexus

SNPshotrs149364215
SNPdbers149364215
MSV3drs149364215
GWAS Ctlgrs149364215
Max Magnitude0
ClinVar
Risk rs149364215(A,T;A,T)
Alt rs149364215(A,T;A,T)
Reference rs149364215(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene ERCC4
CLNDBN Fanconi anemia, complementation group Q
Reversed 0
HGVS NC_000016.9:g.14041518C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049245.28,