ClinVar Miner

List of intergenic variants reported as not provided for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NC_000006.12:g.30806580G>A rs3130783 0.74116
NC_000015.10:g.58396268C>G rs920915 0.54639
NC_000016.10:g.56959412C>A rs3764261 0.31123
NM_001645.3(APOC1):c.*459A>G rs4420638 0.18374
NM_001385.2(DPYS):c.-154C>G rs78426610 0.03517
NM_000895.2(LTA4H):c.*640C>A rs142926035 0.00915
NR_163594.1(SSPO):n.13348A>C rs202144866 0.00473
NR_163193.1(TCP10):n.1018G>A rs140649985 0.00424
NR_163193.1(TCP10):n.943C>T rs200948850 0.00350
NR_163594.1(SSPO):n.15289G>A rs202079888 0.00188
NR_163594.1(SSPO):n.11109T>A rs200844215 0.00128
NM_005732.3(RAD50):c.-352G>A rs104895040 0.00001
GRCh37/hg19 17p11.2(chr17:19515340-19536015)x1
NCBI36/hg18 10p15.3-14(chr10:1-6889456)x1
NCBI36/hg18 16p11.2(chr16:29385560-30239515)x3
NCBI36/hg18 1q21.1(chr1:143639135-144458626)x3
NCBI36/hg18 1q41-44(chr1:214401568-247249719)
NCBI36/hg18 1q42.2(chr1:229779180-229879929)x3
NCBI36/hg18 2p25.3(chr2:1245633-1879818)x3
NCBI36/hg18 6p12.3(chr6:45579286-46089921)x3
NCBI36/hg18 7q11.22(chr7:69313697-69359559)x1
NCBI36/hg18 9p13.2(chr9:36470667-37047553)x3
NC_012920.1(MT-CYB):m.263A>G rs2853515
NM_000249.3(MLH1):c.*281G>T rs104895003
NM_005013.2(NUCB2):c.-427A>C rs186174
NR_163594.1(SSPO):n.8646T>A rs747906568
Single allele

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