ClinVar Miner

List of variants in gene MAX reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_002382.5(MAX):c.*1123A>C rs552459072
NM_002382.5(MAX):c.*1229C>T rs562514408
NM_002382.5(MAX):c.*1278C>T rs541851564
NM_002382.5(MAX):c.*1308C>T rs527697025
NM_002382.5(MAX):c.*144C>T rs191382960
NM_002382.5(MAX):c.*248A>T rs559154342
NM_002382.5(MAX):c.*297C>T rs561525266
NM_002382.5(MAX):c.*344T>A rs561238353
NM_002382.5(MAX):c.*375G>A rs539220905
NM_002382.5(MAX):c.*405G>A rs45440292
NM_002382.5(MAX):c.*603C>G rs117802316
NM_002382.5(MAX):c.*7C>T rs199514174
NM_002382.5(MAX):c.*873T>C rs183467855
NM_002382.5(MAX):c.-100T>G rs111941208
NM_002382.5(MAX):c.-126_-123AGTG[4] rs556734672
NM_002382.5(MAX):c.-18C>T rs201456746
NM_002382.5(MAX):c.-94G>C rs536235832
NM_002382.5(MAX):c.-98G>T rs556543602
NM_002382.5(MAX):c.-99G>A rs570017996
NM_002382.5(MAX):c.177C>G (p.Ser59=) rs781103630
NM_002382.5(MAX):c.21C>A (p.Ile7=) rs760248675
NM_002382.5(MAX):c.279T>C (p.Ala93=) rs145370107
NM_002382.5(MAX):c.295+10C>G rs375446224
NM_002382.5(MAX):c.295+10C>T rs375446224
NM_002382.5(MAX):c.295+8C>G rs754409025
NM_002382.5(MAX):c.351C>T (p.Ser117=) rs1555340215
NM_002382.5(MAX):c.36+10G>C rs1421908769
NM_002382.5(MAX):c.36+9T>C rs774467253
NM_002382.5(MAX):c.375C>T (p.Asn125=) rs370238588
NM_002382.5(MAX):c.384C>A (p.Gly128=) rs1555340201
NM_002382.5(MAX):c.402C>T (p.Phe134=) rs765370870
NM_002382.5(MAX):c.426G>A (p.Ser142=) rs145787299
NM_002382.5(MAX):c.432T>A (p.Ser144=) rs1485899939
NM_002382.5(MAX):c.57A>G (p.Gln19=) rs1395966308
NM_002382.5(MAX):c.63+8T>C rs776724315
NM_002382.5(MAX):c.6C>T (p.Ser2=) rs138539686

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