List of variants in gene ANKRD11 reported as uncertain significance by New York Genome Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.1763C>T (p.Ser588Leu)	rs202142344	0.00029
NM_013275.6(ANKRD11):c.1360G>A (p.Val454Met)	rs149569330	0.00008
NM_013275.6(ANKRD11):c.5315C>T (p.Ser1772Leu)	rs776119333	0.00006
NM_013275.6(ANKRD11):c.4259T>C (p.Ile1420Thr)	rs142828350	0.00005
NM_013275.6(ANKRD11):c.2056G>C (p.Val686Leu)	rs759702780	0.00004
NM_013275.6(ANKRD11):c.2860G>A (p.Ala954Thr)	rs745768322	0.00002
NM_013275.6(ANKRD11):c.1286C>T (p.Ser429Leu)	rs370109948	0.00001
NM_013275.6(ANKRD11):c.4217A>T (p.Tyr1406Phe)	rs943784682	0.00001
NM_013275.6(ANKRD11):c.4471G>A (p.Glu1491Lys)	rs1296165234	0.00001
NM_013275.6(ANKRD11):c.6226C>T (p.Pro2076Ser)	rs1314385190	0.00001
NM_013275.6(ANKRD11):c.-145+15205C>T	rs2057211213
NM_013275.6(ANKRD11):c.-145+4A>T	rs895163510
NM_013275.6(ANKRD11):c.1056C>G (p.Asp352Glu)	rs149211555
NM_013275.6(ANKRD11):c.1357A>G (p.Lys453Glu)	rs2151764903
NM_013275.6(ANKRD11):c.227-269A>G	rs2151799587
NM_013275.6(ANKRD11):c.3653A>C (p.Lys1218Thr)	rs2151753979
NM_013275.6(ANKRD11):c.3725C>T (p.Ala1242Val)
NM_013275.6(ANKRD11):c.4265T>G (p.Leu1422Trp)	rs2151750772
NM_013275.6(ANKRD11):c.4928C>A (p.Pro1643Gln)	rs147690079
NM_013275.6(ANKRD11):c.5681C>G (p.Pro1894Arg)	rs760261187
NM_013275.6(ANKRD11):c.6043T>C (p.Tyr2015His)	rs1395480845
NM_013275.6(ANKRD11):c.7114C>T (p.Arg2372Cys)	rs1192971319

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