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rs672601337

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs672601337(A;G)
Make rs672601337(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position1270774
GeneBHLHA9
is asnp
is mentioned by
dbSNPrs672601337
ebirs672601337
HLIrs672601337
Exacrs672601337
Varsomers672601337
Maprs672601337
PheGenIrs672601337
hapmaprs672601337
1000 genomesrs672601337
hgdprs672601337
ensemblrs672601337
gopubmedrs672601337
geneviewrs672601337
scholarrs672601337
googlers672601337
pharmgkbrs672601337
gwascentralrs672601337
openSNPrs672601337
23andMers672601337
23andMe allrs672601337
SNP Nexus

SNPshotrs672601337
SNPdbers672601337
MSV3drs672601337
GWAS Ctlgrs672601337
Max Magnitude0
ClinVar
Risk rs672601337(G;G)
Alt rs672601337(G;G)
Reference rs672601337(A;A)
Significance Pathogenic
Disease Syndactyly type 9
Variation info
Gene BHLHA9
CLNDBN Syndactyly type 9
Reversed 0
HGVS NC_000017.10:g.1174068A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000149486.5,