RS1107946 COL1A1

Health Risk Chr 17:50203628 snv intron variant

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What This Variant Does

"Current limitations of SNP data from the public domain for studies of complex disorders: a test for ...

Associated Conditions

Bone mineral density variation quantitative trait locus

ClinVar Assertions (1)

NC_000017.11:g.50203629=

· 1 submitter

Population Frequencies

1kG AFR

69.3%

1kG ALL

25.8%

1kG AMR

30%

1kG EAS

30.4%

1kG EUR

13.8%

1kG SAS

76.4%

Other Variants in COL1A1