ClinVar Miner

List of variants in gene FAS reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_000043.6(FAS):c.46G>A (p.Ala16Thr) rs3218619 0.03995
NM_000043.6(FAS):c.369G>A (p.Gln123=) rs28362318 0.00529
NM_000043.6(FAS):c.580G>A (p.Glu194Lys) rs56006128 0.00138
NM_000043.6(FAS):c.*436C>T rs143388574 0.00132
NM_000043.6(FAS):c.*978C>T rs181225729 0.00032
NM_000043.6(FAS):c.958A>G (p.Ser320Gly) rs146209060 0.00028
NM_000043.6(FAS):c.578A>G (p.Lys193Arg) rs150489856 0.00026
NM_000043.6(FAS):c.*70G>C rs80330323 0.00012
NM_000043.6(FAS):c.652-7T>C rs370323285 0.00005
NM_000043.6(FAS):c.444-15T>C rs372996634 0.00004
NM_000043.6(FAS):c.505+17G>A rs767973417 0.00004
NM_000043.6(FAS):c.216C>T (p.Asp72=) rs766429180 0.00003
NM_000043.6(FAS):c.630T>C (p.His210=) rs751973753 0.00003
NM_000043.6(FAS):c.651+8T>C rs771146577 0.00003
NM_000043.6(FAS):c.867A>C (p.Glu289Asp) rs377337130 0.00003
NM_000043.6(FAS):c.945C>T (p.Leu315=) rs1188345187 0.00003
NM_000043.6(FAS):c.519C>T (p.Asn173=) rs1382455258 0.00002
NM_000043.6(FAS):c.57G>A (p.Ser19=) rs757754872 0.00002
NM_000043.6(FAS):c.879A>G (p.Thr293=) rs1413117342 0.00002
NM_000043.6(FAS):c.948G>A (p.Lys316=) rs114502430 0.00002
NM_000043.6(FAS):c.246C>T (p.Cys82=) rs777751533 0.00001
NM_000043.6(FAS):c.270G>A (p.Glu90=) rs745375995 0.00001
NM_000043.6(FAS):c.354C>T (p.Asn118=) rs1266114057 0.00001
NM_000043.6(FAS):c.444-19C>T rs764387025 0.00001
NM_000043.6(FAS):c.506-14G>A rs766198534 0.00001
NM_000043.6(FAS):c.78A>G (p.Gln26=) rs746017530 0.00001
NM_000043.6(FAS):c.798T>C (p.Asn266=) rs758630212 0.00001
NM_000043.6(FAS):c.87C>T (p.Asp29=) rs1323745013 0.00001
NM_000043.6(FAS):c.102A>G (p.Gly34=) rs1554849878
NM_000043.6(FAS):c.140A>G (p.Gln47Arg)
NM_000043.6(FAS):c.144C>T (p.Asn48=)
NM_000043.6(FAS):c.145T>C (p.Leu49=)
NM_000043.6(FAS):c.162T>C (p.His54=)
NM_000043.6(FAS):c.174C>T (p.Phe58=)
NM_000043.6(FAS):c.196+17A>G
NM_000043.6(FAS):c.197-11T>A rs187793393
NM_000043.6(FAS):c.197-11T>C rs187793393
NM_000043.6(FAS):c.197-18C>G rs765687911
NM_000043.6(FAS):c.197-8T>C rs2133501996
NM_000043.6(FAS):c.249G>A (p.Val83=)
NM_000043.6(FAS):c.264G>A (p.Gly88=) rs2133503215
NM_000043.6(FAS):c.31-13T>A
NM_000043.6(FAS):c.324T>C (p.Asp108=) rs1848316008
NM_000043.6(FAS):c.334+11T>C
NM_000043.6(FAS):c.335-10G>T rs377251325
NM_000043.6(FAS):c.335-13A>T
NM_000043.6(FAS):c.335-15A>C
NM_000043.6(FAS):c.33T>C (p.Val11=)
NM_000043.6(FAS):c.345G>A (p.Val115=) rs2133513698
NM_000043.6(FAS):c.396C>T (p.Asn132=)
NM_000043.6(FAS):c.39G>A (p.Thr13=) rs377196867
NM_000043.6(FAS):c.412A>G (p.Thr138Ala)
NM_000043.6(FAS):c.430G>A (p.Asp144Asn) rs753670814
NM_000043.6(FAS):c.432C>T (p.Asp144=) rs574338716
NM_000043.6(FAS):c.443+15T>G
NM_000043.6(FAS):c.443+20T>C
NM_000043.6(FAS):c.444-12T>C
NM_000043.6(FAS):c.444-9T>C
NM_000043.6(FAS):c.477C>G (p.Leu159=)
NM_000043.6(FAS):c.480C>T (p.Thr160=) rs1589482110
NM_000043.6(FAS):c.489C>A (p.Thr163=)
NM_000043.6(FAS):c.505+14T>C
NM_000043.6(FAS):c.505+16C>A
NM_000043.6(FAS):c.558A>G (p.Leu186=)
NM_000043.6(FAS):c.588G>A (p.Gln196=)
NM_000043.6(FAS):c.642T>G (p.Thr214=)
NM_000043.6(FAS):c.652-9G>T rs1848622815
NM_000043.6(FAS):c.66T>C (p.Ser22=)
NM_000043.6(FAS):c.676+13T>A
NM_000043.6(FAS):c.677-16A>G
NM_000043.6(FAS):c.677-9A>G
NM_000043.6(FAS):c.684C>T (p.Asp228=) rs1848665121
NM_000043.6(FAS):c.711T>C (p.Ala237=)
NM_000043.6(FAS):c.753G>A (p.Lys251=)
NM_000043.6(FAS):c.768A>G (p.Glu256=)
NM_000043.6(FAS):c.801C>T (p.Val267=)
NM_000043.6(FAS):c.867A>G (p.Glu289=) rs377337130
NM_000043.6(FAS):c.870G>A (p.Ala290=)
NM_000043.6(FAS):c.909T>C (p.Leu303=) rs967060461
NM_000043.6(FAS):c.915T>G (p.Thr305=)
NM_000043.6(FAS):c.978C>T (p.Asn326=)
NM_000043.6(FAS):c.993C>A (p.Ile331=) rs1237891648

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