ClinVar Miner

List of variants in gene FAS reported as benign for autoimmune disease

Included ClinVar conditions (81):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000043.6(FAS):c.642T>C (p.Thr214=) rs2234978 0.72086
NM_000043.6(FAS):c.*1084C>T rs1468063 0.16498
NM_000043.6(FAS):c.*565A>T rs1051070 0.07031
NM_000043.6(FAS):c.46G>A (p.Ala16Thr) rs3218619 0.03995
NM_000043.6(FAS):c.222A>G (p.Thr74=) rs2229521 0.03925
NM_000043.6(FAS):c.*765T>C rs9658776 0.03922
NM_000043.6(FAS):c.*142A>G rs9658774 0.02166
NM_000043.6(FAS):c.141G>A (p.Gln47=) rs3218621 0.02156
NM_000043.6(FAS):c.505+16C>T rs3218620 0.01048
NM_000043.6(FAS):c.365C>T (p.Thr122Ile) rs3218614 0.00774
NM_000043.6(FAS):c.183G>A (p.Lys61=) rs3218613 0.00606
NM_000043.6(FAS):c.369G>A (p.Gln123=) rs28362318 0.00529
NM_000043.6(FAS):c.550A>G (p.Ile184Val) rs28362322 0.00324
NM_000043.6(FAS):c.33T>A (p.Val11=) rs113022949 0.00135
NM_000043.6(FAS):c.*638T>C rs192032778 0.00117
NM_000043.6(FAS):c.103T>C (p.Leu35=) rs9333296 0.00083
NM_000043.6(FAS):c.*1333G>T rs9658779 0.00071
NM_000043.6(FAS):c.*1203G>A rs190060976 0.00062
NM_000043.6(FAS):c.505+14T>G rs76988052 0.00038
NM_000043.6(FAS):c.578A>G (p.Lys193Arg) rs150489856 0.00026
NM_000043.6(FAS):c.*582T>G rs542335688 0.00023
NM_000043.6(FAS):c.*84G>A rs754986111 0.00020
NM_000043.6(FAS):c.*853C>T rs770098016 0.00010
NM_000043.6(FAS):c.*174A>G rs776971935 0.00007
NM_000043.6(FAS):c.78A>G (p.Gln26=) rs746017530 0.00001
NM_000043.6(FAS):c.444-5del rs751798922
NM_000043.6(FAS):c.444-5dup rs751798922

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.