Product Details

SNP ID
rs1974955
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:49779866 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTCCTGTGTTTTCTCATGGTGTTC[A/C]CTCTGCATCTGTCTGTGTCCACATC
Phenotype
MIM: 611108
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
VWC2 PubMed Links

Gene Details

Gene
VWC2
Gene Name
von Willebrand factor C domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_198570.4 Intron NP_940972.2

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