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rs2071676 has not been reported to ClinVar. Refer to dbSNP record rs2071676 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs2071676

Clinical significance: not reported in ClinVar
Reference allele: G
Variation allele: A
Variation type: single nucleotide variation

Organism: Homo sapiens
GRCh38.p14: NC_000009.12: 35,674,055
GRCh37.p13: NC_000009.11: 35,674,052

Genome Data Viewer

Source: KnownItemSensor

The following term was not found in ClinVar: rs2071676.
No items found.