List of variants in gene SLC4A11 reported as uncertain significance by Natera, Inc.

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001174089.2(SLC4A11):c.2176G>A (p.Gly726Arg)	rs143965185	0.00029
NM_001174089.2(SLC4A11):c.1635G>A (p.Thr545=)	rs201133609	0.00023
NM_001174089.2(SLC4A11):c.501C>T (p.Ala167=)	rs749352950	0.00021
NM_001174089.2(SLC4A11):c.523+9G>A	rs200962876	0.00013
NM_001174089.2(SLC4A11):c.2340C>T (p.Leu780=)	rs199634796	0.00012
NM_001174089.2(SLC4A11):c.1959C>A (p.Ser653=)	rs140234175	0.00007
NM_001174089.2(SLC4A11):c.1049T>C (p.Ile350Thr)	rs370322948	0.00003
NM_001174089.2(SLC4A11):c.1158C>T (p.Asp386=)	rs764910925	0.00003
NM_001174089.2(SLC4A11):c.390C>T (p.Thr130=)	rs149548266	0.00003
NM_001174089.2(SLC4A11):c.1489+8C>T	rs760670114	0.00001
NM_001174089.2(SLC4A11):c.384G>A (p.Thr128=)	rs761675091	0.00001
NM_001174089.2(SLC4A11):c.1168+10T>G	rs1439498080
NM_001174089.2(SLC4A11):c.1782C>T (p.Asp594=)	rs2067673861
NM_001174089.2(SLC4A11):c.2331C>A (p.Leu777=)	rs1568527712

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