ClinVar Miner

List of variants in gene combination HBD, LOC106099063 reported as other

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
NM_000519.3(HBD):c.110C>A (p.Pro37His) rs34383555
NM_000519.3(HBD):c.130G>A (p.Glu44Lys) rs35166721
NM_000519.3(HBD):c.131A>G (p.Glu44Gly) rs36084266
NM_000519.3(HBD):c.143A>T (p.Asp48Val) rs34977235
NM_000519.3(HBD):c.155C>G (p.Pro52Arg) rs34489183
NM_000519.3(HBD):c.174C>A (p.Asn58Lys) rs35666685
NM_000519.3(HBD):c.208G>C (p.Gly70Arg) rs35913713
NM_000519.3(HBD):c.226C>G (p.Leu76Val) rs34430836
NM_000519.3(HBD):c.265C>G (p.Leu89Val) rs34933313
NM_000519.3(HBD):c.272A>T (p.Glu91Val) rs34420481
NM_000519.3(HBD):c.280T>G (p.Cys94Gly) rs28933077
NM_000519.3(HBD):c.295G>A (p.Val99Met) rs28933076
NM_000519.3(HBD):c.298G>A (p.Asp100Asn) rs35329985
NM_000519.3(HBD):c.315G>T (p.Arg105Ser) rs34390965
NM_000519.3(HBD):c.74G>A (p.Gly25Asp) rs34460332
NM_000519.3(HBD):c.77G>A (p.Gly26Asp) rs34389944
NM_000519.3(HBD):c.81G>C (p.Glu27Asp) rs34289459
NM_000519.3(HBD):c.82G>T (p.Ala28Ser) rs35152987

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.